Recalls: week of Aug 10–16, 2026
75 recalls dated Aug 10–16, 2026, from the CPSC, FDA, USDA and NHTSA, each explained in plain English. 28 are rated “stop using now”.
Food — 15
- Ferrero USA recalls Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz
Ferrero USA recalls Fannie May & XO Marshmallow Pixie S'mores Collection (4.47oz) sold 8/7-8/14/2026 due to undeclared milk and pecans. Consumers should check best by dates and contact Ferrero for details.
- THE HAMPTON GROCER recalls THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS +
The Hampton Grocer recalls small batch lactation granola pouches due to potential Salmonella contamination. Consumers should check product labels for lot codes and expiration dates to determine if affected.
- Gifford's Dairy, Inc. recalls Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7
Gifford's HomeMaine POWER PLAY FUDGE ice cream (1 quart) recalled due to potential rubber pieces. Consumers should check UPC 8 60864 00030 7 and lot code 26184 for affected products.
- Prince Bakery Inc recalls Prince Sesame FRENCH BREAD; LONG FRENCH; Net Wt. 10 oz (284g); INGREDIENTS: ENRICHED BLEACHED FLOUR, (WHEAT FLOUR, MALT
Prince Bakery recalls sesame French bread due to sesame seeds not being declared on ingredient labels. This affects products with UPC 8 93601 00100 8 sold in red and yellow bags.
- Prince Bakery Inc recalls Prince PAN DE MANTECA; SPANISH STYLE; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT
Prince Bakery recalls Spanish-style 8oz bread due to milk not being listed in ingredients. This affects consumers who require milk labeling for dietary needs.
- Prince Bakery Inc recalls Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY
Prince Bakery recalls Italian bread with sesame seeds that were not properly listed on the ingredient label. This may cause confusion for people with sesame allergies.
- Prince Bakery Inc recalls Prince ITALIAN BREAD; Sesame; ITALIAN & FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); INGREDIENTS: ENRICHED BLEACHED
Prince Bakery recalls Italian bread products due to sesame seeds not being declared on ingredient labels, potentially causing allergic reactions for those with sesame allergies.
- Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc. recalls Product is Potato Sourdough Bread and sold under three following names: Potato Market Loaf 20oz. UPC 733163001576,
Grand Central Bakery recalls potato sourdough bread products due to potential metal pieces. Consumers should check labels for specific product names and UPCs to determine if affected.
- Byron White Formulas, Inc. recalls Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White
Byron White recalls A-L Complex Herbal Supplements that may contain nuts due to label not declaring nuts in English. Consumers should check lot codes for affected products.
- Byron White Formulas, Inc. recalls Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas
Byron White Formulas recalls herbal supplements that may contain nuts but lack English labeling for allergen warnings.
- CUISINE, KETTLE recalls Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14
Marketside Tomato Bisque Soup Kit recalled due to presumptive positive Listeria monocytogenes test. Keep refrigerated until use by 8/22/2026.
- Byron White Formulas, Inc. recalls Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White
Byron White Formulas A-FNG Herbal Supplements (1.0 fl. oz.) may contain nuts but label does not declare walnuts in English. Consumers should check lot codes for affected products.
- Africando Foods LLC recalls Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICANDO FOODS, LLC ALFREDO HOT
Africando Foods LLC recalls Alfredo hot sauce bottles for missing wheat and soybean oil on ingredient labels. This minor labeling issue may affect consumers who require full ingredient transparency.
- UPSTATE NIAGARA COOPERATIVE recalls Mehadrin Chocolate Leben; 6 OZ (170g) CUPS, UPC: 070784023144
Upstate Niagara Cooperative recalls Mehadrin Chocolate Leben 6oz cups due to possible improper pasteurization. Consumers should check UPC 070784023144 and lot code 101426 L5 2W for affected products.
- Lidl US TRADING recalls VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTRIBUTED BY LIDL US, LLC ARLINGTON, VA
Lidl recalls VITASIA Asian Style Wok Spice Mix (UPC 4335619355491) due to Salmonella contamination. Consumers should check product details and follow official recall steps.
Consumer products — 18
- Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash Hazard; Violates Mandatory Standard for ATVs
Yamazuki recalls youth ATVs model XW-A19 due to parking brakes failing and speed limiters not set for children over 6, risking serious injury or death in crashes. Consumers must stop using immediately and get a free repair kit.
- TooyBing Wooden Bead Stacking Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Small Parts Ban
TooyBing Wooden Bead Stacking Toys (model TB-MZWJ) recalled due to choking hazard for children under 3. Stop using immediately and follow destruction steps for replacement.
- Taleco Gear Recalls Baby Jumpers, Baby Swings and 2-in-1 Baby Jumper & Swings Due to Risk of Serious Injury or Death from Fall and Strangulation Hazards
Taleco Gear recalls baby jumpers, swings and 2-in-1 jumpers/swings due to fall and strangulation hazards. Consumers must stop using immediately and get a refund.
- Sunnyside Corporation Recalls 1-K Kerosene Heater and Appliance Fuel Containers Due to Risk of Serious Injury or Death from Flash Fire and Burn Hazard; Violates Mandatory Standards for Portable Fuel Containers
Sunnyside recalls 1-K kerosene fuel containers due to flash fire and burn hazards from missing safety features. Consumers must stop using immediately and return for refund.
- SUGIFT Recalls SUGIFT Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
SUGIFT recalls 13 electric pressure washers due to missing GFCI protection and risk of shock/electrocution. Consumers must stop using immediately and destroy the unit by cutting power cord.
- Southern Telecom Recalls Brookstone-Branded Tabletop Fire Pits Due to Risk of Serious Burn Injury or Death from Flame Jetting and Fire Hazards
Southern Telecom recalls Brookstone Tabletop Fire Pits with model numbers BSFIREPIT01-03 due to risk of serious burns from uncontrolled flames and flame jetting. Consumers must stop using and dispose of these products immediately.
- Shengsen Prank Sound Makers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Shengsen Toys
Shengsen Prank Sound Makers recalled due to risk of serious injury or death from children swallowing lithium batteries. Products sold with coin batteries lack required safety warnings.
- Ritchey Design Recalls Carbon Bicycle Forks Due to Risk of Serious Injury or Death from Fall and Crash Hazards
Ritchey recalls carbon bicycle forks with a loose alloy insert that can cause accessories to fall and lead to serious injury or death during falls or crashes. Consumers must stop using affected forks immediately and register for a free closure kit.
- Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Qabefy
Qabefy mattresses sold on Amazon violate flammability standards, risking fire injury or death. Consumers must stop using immediately and destroy the mattress by marking it with 'Recalled' and date before disposal.
- Hampton Bay Halwin 52-Inch Ceiling Fans Recalled Due to Impact and Injury Hazards; Manufactured by Youngo Limited
Hampton Bay Halwin 52-inch ceiling fans with model AK396H-MBK and AK396H-BN are recalled due to risk of fan blades separating from motor, causing injury. Consumers must stop using immediately and contact Youngo for refund or store credit.
- Goody King Magnetic Building Cubes and Blocks Recalled Due to Risk of Serious Injury or Death from Magnetic Ingestion Hazard; Imported by Yi Suen Commerce
Goody King Magnetic Building Cubes and Blocks recalled due to magnets that can become loose and cause serious injury or death if swallowed by children. Consumers must stop using and return for refund.
- GigaCloud Technology USA Recalls Merax Murphy Beds Due to Risk of Serious Injury or Death from Impact and Crush Hazards
GigaCloud Technology recalls Merax Murphy beds with model numbers GX000392AAK, GX000391AAK, and GX000383AAK due to risk of falling frames during assembly causing serious injury. Consumers must stop using immediately and contact for free repair.
- Fastbuy Recalls Zimtown Portable Gas and Fuel Cans Due to Risk of Serious Injury or Death from Burn Hazard and Child Poisoning; Violate Mandatory Standard for Portable Fuel Containers
Zimtown recalls portable gas and fuel cans due to child-unfriendly closures causing burn and poisoning risks. Stop using immediately and contact for refund.
- DUMOS Nine-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
DUMOS Nine-Drawer Dressers sold without wall anchoring pose tip-over and entrapment risks for children. Recalled units must be destroyed by cutting drawers and marking as recalled.
- Deli Jerry Fuel Containers Recalled Due to Risk of Serious Injury or Death from Burn Hazard and Child Poisoning; Violate Mandatory Standard for Portable Fuel Containers; Sold on Walmart.com by Deli OfficeSupplies
Deli Jerry fuel containers recalled due to child poisoning and burn hazards from non-child-resistant closures. Stop using immediately and return for refund.
- CuberShop Magnetic Speed Cubes Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Imported by SKY CUBE HK
CuberShop's Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled due to loose high-powered magnets that can cause serious injury or death if swallowed by children. Consumers must stop using and dispose of magnets safely.
- Cooluli Recalls 10-Liter and 15-Liter Minifridges Due to Fire and Burn Hazards
Cooluli 10L and 15L minifridges with faulty electrical switches risk fire and burns. Stop using immediately and get a free replacement power cord via www.cooluli.com/pages/product-notices-recalls.
- COMMOWNER Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by AZ Home Concept
1,694 COMMOWNER electric pressure washers (models HD14P-Z, HX18) recalled due to missing ground-fault circuit-interrupter (GFCI) causing shock or electrocution risks. Consumers must stop use and destroy units by cutting power cord.
Vehicles — 4
- CHRYSLER PACIFICA (2027) recall — Back Over Prevention
Chrysler recalls 2026-2027 Pacifica models due to rearview camera image failures that could increase crash risk. Owners must update software via dealer or OTA to fix the issue.
- JEEP GRAND CHEROKEE L (2026) recall — Visibility
Chrysler recalls 2026 Jeep Grand Cherokee L vehicles with faulty windshield wiper software that may cause wipers to fail, increasing crash risk. Owners must update BCM software by September 2026.
- NISSAN ALTIMA (2025) recall — Air Bags
Nissan recalls certain 2025 Altima vehicles due to front passenger air bags potentially not deploying in crashes. Owners must have air bag mounting fasteners replaced by dealers at no cost.
- CHEVROLET SILVERADO 2500 (2025) recall — Tires
Chevrolet is recalling 2024-2025 Silverado 2500 models with 20-inch tires for incorrect pressure labels causing underinflated tires. Owners must have tires inspected and TPMS relearned free by dealers.
Drugs — 15
- Allies Group Inc. recalls THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl.
Allies Group recalls The One SPF 50 Invisible Sunscreen Gel (20ml) that may not provide reliable SPF 50 protection. Consumers should check product details and contact Allies Group for guidance.
- Allies Group Inc. recalls THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 50ML - 1.7 fl.
Allies Group recalls SPF 50 Invisible Sunscreen Gel (50ml) that may not reliably provide stated SPF 50 protection. Consumers should check product details and contact Allies Group for guidance.
- Allies Group Inc. recalls THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 90ml - 3 fl.
Allies Group recalls their SPF 50 Invisible Sunscreen Gel (90ml) because it may not provide reliable SPF 50 protection. Consumers should check product details and contact the company for guidance.
- Allies Group Inc. recalls THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 3ml - 0.1 fl.
Allies Group recalls their SPF 50 Invisible Sunscreen Gel (3ml) because it may not provide reliable SPF 50 protection. Affected products have specific lot numbers and expiration dates. Consumers should check labels and contact Allies Group for details.
- Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 2.5 mg per 5 mL, Delivers: 5 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. This medication may degrade over time, potentially affecting safety. Consumers should check product details and contact the manufacturer for instructions.
- Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 5 mg per 1 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. This medication may degrade over time, potentially affecting safety and effectiveness.
- Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 5 mg per 10 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. This medication may degrade over time, posing risks to safety. Check NDC codes and expiration dates for affected lots.
- Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 10 mg per 2 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. This medication may degrade over time, posing risks to safety. Check NDC codes and expiration dates for affected batches.
- Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 20 mg per 4 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. This medication may degrade over time, potentially affecting safety. Check NDC codes and expiration dates for affected lots.
- Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 15 mg per 3 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. Products may degrade over time, risking ineffective treatment. Check NDC codes and expiration dates for affected items.
- Apotex Corp. recalls Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufactured by: Apotex Inc.,
Apotex recalls 37.5mg Paxil CR tablets due to failing 24-month stability tests. This may affect medication safety. Check your prescription bottle for NDC 60505-4379-3.
- B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA
B. Braun Medical recalls Lactated Ringer's Injection USP 1000mL (L7500) due to particulate matter. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
- American Regent, Inc. recalls Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial, Rx Only, For Intravenous Infusion,
American Regent recalls epinephrine injections with particulate matter and lack of sterility. Affected lots expire August 2026 through July 2027. Stop using immediately if you have these vials.
- Fresenius Kabi USA, LLC recalls Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA,
Fresenius Kabi recalls Tyenne (tocilizumab-aazg) injection due to glass particles found in some batches. This may cause serious injury if injected. Affected units have specific lot numbers and expiration dates.
- Church & Dwight Co., Inc. recalls Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free
Church & Dwight recalls Zicam Cold Remedy nasal swabs due to microbiological testing failures found during FDA inspection. Affected lots have specific expiration dates and UPC codes.
Medical devices — 23
- Straumann USA LLC recalls GM Helix Implant, REF: 109.984;
Straumann recalls GM Helix Implant REF: 109.984 due to packaging dimensions not matching the actual implant. Affected units may have incorrect size specifications.
- Abiomed, Inc. recalls Impella Optical Controller, Automated Impella Controller, Impella Connect Package with the below product descriptions
Abiomed recalls Impella Optical Controller, Automated Impella Controller, and Impella Connect Package units with specific product codes and serial numbers due to potential purge cassette recognition issues from purge flag component failure.
- Abiomed, Inc. recalls Impella Optical Controller with the below product descriptions and corresponding Product Codes. 1. Impella Optical
Abiomed recalls Impella Optical Controller units with specific product codes and serial numbers due to potential purge cassette recognition issues from purge flag component failure.
- Abiomed, Inc. recalls Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella
Abiomed recalls Impella Controllers with specific product codes and serial numbers due to potential purge cassette recognition issues from purge flag component failure.
- Medline Industries, LP recalls Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL LINE ST JOES SYR PACK,
Medline recalls two convenience kits due to potential fungal contamination in specific lots. Contaminated kits may cause serious infections or death if used improperly.
- Medline Industries, LP recalls Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3)
Medline recalls specific convenience kits due to potential fungal contamination that could cause serious infections or death. Affected kits include models ACC010308A, ACC010374A, and others with certain lot numbers.
- Medline Industries, LP recalls Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number: DYNDB3100; 3)
Medline recalls convenience kits with fungal contamination risk. Kits may contain Aspergillus penicillioides leading to serious health issues. Check product catalog numbers and lot numbers for affected items.
- Medline Industries, LP recalls Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number:
Medline recalls specific convenience kits due to potential fungal contamination in certain lots, which may cause serious infections or death if used improperly.
- Medline Industries, LP recalls Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number: DYNDH1487A
Medline recalls two convenience kit models due to potential fungal contamination that could cause serious infections or death. Affected kits contain specific lot numbers and catalog codes.
- Medline Industries, LP recalls Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
Medline recalls specific anesthesia L&D kits due to potential fungal contamination from Aspergillus penicillioides, which can cause serious infections or death. Affected kits have catalog numbers DYKMBNDL199A and specific lot numbers.
- Medline Industries, LP recalls Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A
Medline recalls two convenience kit models due to potential fungal contamination that could cause serious infections or death. Affected kits include specific catalog numbers and lot numbers.
- Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
Baxter recalls Novum IQ Syringe Pump model 40800BAXUSL due to software issue that may cause infusion errors when syringes are replaced during multi-syringe infusions. Affected units have specific serial numbers.
- Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Baxter recalls Novum IQ Syringe Pump model 4080: software issue may cause infusion errors if syringe reaches empty during multi-syringe infusions. Affected units have specific serial numbers and model numbers.
- Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF:
Bard Access Systems recalls specific DuoGlide short-term dialysis catheters due to a downstream class I recall. Affected models include straight and curved extensions with reference numbers 5625150-5626240. This recall addresses safety concerns from a prior class I recall.
- AVID Medical, Inc. recalls Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;
Haylard's Continuous Nerve Block Tray (Model BMCN001-05) with specific sodium chloride ampule lots may have sterility issues. Affected users should check their kit lots and contact AVID Medical for details.
- Bard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis
Bard Access Systems recalls specific Power-Trialysis Short-Term Dialysis Catheters due to a downstream class I recall. Affected models include straight and curved catheters with reference numbers starting with 5605150, 5605200, etc. No remedy is listed in the recall notice.
- AVID Medical, Inc. recalls Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;
AVID Medical recalls Haylard Basic Biopsy Trays with model PM415 due to potential sterility issues with sodium chloride ampules. Affected kits may not be safe for medical use.
- AVID Medical, Inc. recalls Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03;
AVID Medical recalls Haylard UNIV IMAGING BIOPSY TRUCUSTOM kits (model VARV042-03) due to potential sterility issues with Sodium Chloride ampules. Affected kits include specific lots and UDI-DI numbers.
- AVID Medical, Inc. recalls Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
AVID Medical recalls Haylard 18G Single Shot Epi Tray (DPGE002-02) due to potential sterility issues with Sodium Chloride ampules. Affected kits may contain recalled ampules from specific lots.
- Fresenius Medical Care Renal Therapies Group, LLC recalls 5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
Fresenius Medical Care recalls 5008X HD/HDF machines with CLiC Blood Tubing Set part 03-5300-3C due to risk of blood leaks during dialysis causing blood loss and hypovolemia. Affected units include specific lots and UDI-DI numbers.
- Fresenius Medical Care Renal Therapies Group, LLC recalls 5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
Fresenius Medical Care recalls 5008X HD/HDF Standard Blood Tubing Sets with part number 03-5300-3 due to risk of blood leaks during dialysis treatment, potentially causing blood loss and hypovolemia.
- Fresenius Medical Care Renal Therapies Group, LLC recalls 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
Fresenius Medical Care recalls 5008X Standard HD Pre-Flush Standard Blood Tubing Set (Part 03-5110-6) due to heightened risk of blood leaks during dialysis treatment, potentially causing blood loss and hypovolemia.
- Fresenius Medical Care Renal Therapies Group, LLC recalls 5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
Fresenius Medical Care recalls 5008X HD/HDF machines with Twister Blood Tubing Set (part 03-5350-8) due to risk of blood leaks during dialysis treatment, potentially causing blood loss and hypovolemia.
What to do if you have a recalled product
- Open the recall and check the model, lot or date codes — only those units are affected.
- Stop using it if it’s rated “stop using now”, and follow the remedy (refund, repair or replacement) on the recall page.
- Got a car? Check it by VIN — vehicle recall repairs are free by law.