Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,021 found- Stop using nowMedical device
Cadwell Industries Inc recalls Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number: 190296-200 UDI-DI code: 00840067100653
Cadwell Industries recalls 23 IOMAX Cortical Modules with defective printed circuit boards that may deliver unintended electrical stimulation. Affected units have specific serial numbers and were sold worldwide. Stop using immediately.
IOMAXAug 18, 2026 - Lower riskMedical device
Radiometer Medical ApS recalls The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and
Radiometer recalls ABL90 FLEX analyzers with software versions 3.6 or lower that may produce inaccurate blood test results. Affected units were sold nationwide in the US from 2026.
RadiometerAug 18, 2026 - Stop using nowMedical device
Stryker Sustainability Solutions recalls BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
Stryker recalls Bard EP XT Decapolar Steerable Catheters with potential breached sterile barrier. This may cause infection, blood clots, or tissue damage. Stop using immediately if you have the specific lot.
StrykerAug 18, 2026 - Use cautionMedical device
Wright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System
Wright Medical Technology recalls 34 Charlotte Claw Screws (Lot 1826666) distributed August 2025-April 2026. Missing threads may cause surgery delays or alternative procedures.
Wright Medical TechnologyAug 18, 2026 - Lower riskMedical device
Philips North America Llc recalls Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333
Philips recalls 62 units of Spectral CT 7500 scanners with software V5.2.x due to potential extra radiation exposure from bolus tracking errors. Affected units sold in U.S. and territories.
PhilipsAug 18, 2026 - Use cautionMedical device
Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number:
Cardinal Health recalls 2957 gyn laparoscopy kits with potential fluid leakage from handpieces that could cause slips and falls. Affected kits have specific catalog numbers and lot numbers.
Cardinal HealthAug 18, 2026 - Use cautionMedical device
Percussionaire Corporation recalls Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC
Percussionaire Corporation recalls Intrapulmonary Percussive Ventilation (IPV) HC due to risk of altered anesthetic delivery causing hypertonia, hypotonia, tachycardia, bradycardia, elevated intracranial pressure, or awareness during anesthesia.
Percussionaire CorporationAug 18, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and
Baxter Healthcare recalls PRO+ 40" MRS SURFACE mattresses with AMT technology due to UDI label errors that may cause incorrect bed frame selection. Affected units have specific serial numbers and model numbers.
Baxter HealthcareAug 18, 2026 - Lower riskDrug
Sage Products, LLC recalls 2% Chlorhexidine Gluconate* Cloth, Non-sterile, 6 Disposable cloths, Sage Products LLC, 3909 Three Oaks Road, Cary,
Sage Products LLC recalls 6-pack of non-sterile 2% chlorhexidine gluconate cloth due to cross contamination risk. Affected items have specific NDC and lot numbers.
Sage ProductsAug 18, 2026 - Lower riskMedical device
Olympus Corporation of the Americas recalls POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting &
Olympus recalls POWERSEAL 5mm 23cm curved jaw sealers due to potential mislabeling as 37cm devices. Affected units may be confused with larger models.
OlympusAug 18, 2026 - Use cautionFood
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper
Dreyer's Grand recalls 24-count Outshine Fruit Bars (strawberry, pineapple, grape, tangerine) due to potential glass pieces. Products may contain glass, posing a choking hazard. Check UPC 041548816678 for affected items.
Dreyer's GrandAug 18, 2026 - Lower riskMedical device
Microgenics Corporation recalls MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, REF: OPRO-101; MAS Omni IMMUNETM PRO Liquid
Microgenics recalls MAS Omni IMMUNE PRO Liquid Assayed Control (Lot OPRO29061A) due to low Parathyroid Hormone recovery risks in test results. Affected units sold worldwide in 2026.
MicrogenicsAug 17, 2026 - Stop using nowFood
The Better Bakehouse Snack Company recalls Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC
The Better Bakehouse Snack Co. recalls Donutful Chocolate Dipped Vanilla Cake Donuts because they contain undeclared milk, posing an allergy risk.
The Better Bakehouse Snack CompanyAug 17, 2026 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Revised C-Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223;
Siemens Healthcare recalls Atellica CH Revised C-Reactive Protein tests with potential for falsely elevated results. All units are affected. Contact for remedy.
Siemens HealthcareAug 17, 2026 - Stop using nowMeat & poultry
Asian America Trading, Inc. Recalls Ineligible Siluriformes Fish Products Imported From the People’s Republic of China
Asian America Trading recalls ready-to-eat fish skin products imported from China. Do not consume; discard or return to retailer.
Asian America TradingAug 17, 2026 - Stop using nowMeat & poultry
Indus Foods, LLC DBA Gangothri Foods Recalls Ready-To-Eat Pickled Goat and Chicken Products Produced Without Benefit of Inspection
Gangothri Foods recalls ~1,626 lbs of pickled goat and chicken products produced without USDA inspection. Do not consume; return or discard.
Gangothri FoodsAug 17, 2026 - Use cautionPet food
Oma’s Pride – Canine Food: Contaminated with Salmonella
Oma's Pride is recalling one lot of Woof Complete Canine Chicken Recipe due to Salmonella contamination. Stop using immediately and contact for refund.
Oma's PrideAug 17, 2026 - Stop using nowFood
Best Friends Bakery, LLC recalls PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHOLE GRAIN OATS, MILK, MARGARINE***WATER, SALT, CONTAINS LESS
Best Friends Bakery recalls 1,416 units of Pumpkin Spice No Bake Cookies due to undeclared peanuts. Check your UPC and lot number.
Best Friends BakeryAug 17, 2026 - Lower riskDrug
Mylan Pharmaceuticals Inc recalls Prasugrel Tablets, USP, 10mg, Rx only, 30 Tablets in each bottle, Manufactured for: Mylan Pharmaceuticals Inc.,
Mylan recalls 10mg Prasugrel tablets that failed 18-month stability testing. These tablets may not be safe for long-term use. Consumers should contact Mylan for details.
MylanAug 17, 2026 - Stop using nowDrug
Baxter Healthcare Corporation recalls Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA,
Baxter recalls 2000mL dextrose injection bags with stainless steel particles. Stop using immediately due to potential serious injury from particulate matter in IV solutions.
Baxter HealthcareAug 17, 2026 - Stop using nowDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare
Baxter recalls 500mL saline injections in VIAFLEX plastic containers due to fiberglass particulates. Stop using if you have these containers with specific lot numbers.
Baxter HealthcareAug 17, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Rollator, Bariatric, Basic Steel, Blue, mechanical walker with four legs and a metal frame intended for medical
Medline recalls 835 bariatric rollators due to front wheel detachment risk. Check lot numbers and stop use immediately if affected.
MedlineAug 14, 2026 - Stop using nowMedical device
American Nitrile Operations Llc recalls Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number: 72-RM50601,72-RM50602,
American Nitrile Operations recalls Performance Pro blue nitrile examination gloves (lots AO01306, etc.) due to tears and debris that may cause infection or chemical exposure.
Performance ProAug 14, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
Medline recalls 771,127 Basic Homecare Beds due to fire risk from hand control pendant overheating. Affected beds may smoke, spark, melt or catch fire. Stop using immediately.
MedlineAug 14, 2026 - Stop using nowFood
Ferrero USA recalls Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz
Ferrero USA recalls Fannie May & XO Marshmallow Pixie S'mores Collection due to undeclared milk and pecans. Check your best by code.
Fannie May & XOAug 14, 2026 - Lower riskDrug
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 GroupAug 14, 2026 - Use cautionFood
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.
The Hampton GrocerAug 14, 2026 - Lower riskFood
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.
Gifford'sAug 14, 2026 - UnratedMedical device
Becton Dickinson & Co. recalls BD Phoenix Panel NMIC-312. Catalog Number: 449082.
Becton Dickinson recalls 553,625 BD Phoenix Panel NMIC-312 units due to potential Klebsiella pneumoniae ATCC BAA-1705 contamination in CPO Ambler classification feature.
Becton DickinsonAug 13, 2026 - Use cautionVehicle
FORD EXPLORER (2026) recall — Engine And Engine Cooling
Ford is recalling 2026 Explorer vehicles with 2.3L engines due to potential engine failure causing loss of drive power and fire risk from oil leaks. Owners must have engine long blocks replaced free by dealers.
FordAug 13, 2026
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