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
35,004 found- Use cautionFood
Slade Gorton & Company, Inc. recalls GOURMET BAY Haddock with Seafood Stuffing; 6oz; SELL BY 05/26/21; LOT# 100457657; KEEP FROZEN; Cooking Instructions:
Slade Gorton recalls 6oz Gourmet Bay Haddock with Seafood Stuffing (lot #100457657, sell by 05/26/21) due to potential Listeria monocytogenes contamination. Keep frozen until 05/26/21.
Slade GortonDec 3, 2019 - Lower riskFood
Mrs. Condies Salad Company, Incorporated recalls Mrs. Condies Salad Company's Honey Bear Small Party Platter containing Ranch Dressing dip,3.5 lbs.
Mrs. Condies Salad Company recalls Honey Bear Small Party Platters with Ranch Dressing dip that contains undeclared milk. Consumers should check labels for the best by date and avoid products with milk not listed in ingredients.
Mrs. Condies Salad CompanyDec 3, 2019 - Use cautionVehicle
FREIGHTLINER CASCADIA (2016) recall — Steering
Daimler Trucks North America recalls 2013-2016 Freightliner Cascadia trucks with Hendrickson 5" drop axles for potential tie-rod tube failure causing loss of steering. Free replacement of parts available.
Daimler Trucks North AmericaDec 2, 2019 - Lower riskMedical device
3-D Matrix, Inc. recalls PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
3-D Matrix recalls PuraSinus Absorb: Nasal Hemostat (part 651-006) due to unvalidated transport boxes. Affected units may have shipping risks.
3-D MatrixDec 2, 2019 - Lower riskMedical device
Argon Medical Devices, Inc recalls BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product
Argon Medical Devices recalls BioPince Full Core Biopsy Instruments due to incorrect labeling. This may cause confusion in medical use. Consumers should contact the manufacturer for details.
Argon Medical DevicesDec 2, 2019 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit,
Medical Action Industries recalls certain CVC Clear Sequence Change Kits due to saline solution pH potentially exceeding USP standards (4.5-7.0). Affected kits include specific models and lot numbers listed in the recall notice.
Medical Action IndustriesDec 2, 2019 - Lower riskMedical device
Medela Inc recalls Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224. The Invia Foam Dressing Kit with FitPad consists
Medela recalls Invia Foam Dressing Kit with FitPad X-Large (3 pcs) SKU #0876224 due to potential holes in sterile packaging. This could compromise sterility during medical use. Affected units were sold with specific expiration dates.
MedelaDec 2, 2019 - Lower riskMedical device
Degania Silicone, Ltd. recalls Medline Thermistor Foley Catheter 14 FR 5-10 ml, non sterile Catalog Number: 102201101463MD {Medline code 55346)
Medline recalls silicone catheters with temperature deviation issues. Affected units may not accurately monitor bladder temperature. Contact Medline for details.
Degania SiliconeDec 2, 2019 - Use cautionMedical device
Thoratec Corp. recalls HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when
Thoratec recalls HeartMate 3 Mobile Power Unit models with specific serial numbers due to static electricity causing power loss that may reduce blood flow from the assist system.
ThoratecDec 2, 2019 - Use cautionMedical device
Polymer Technology Systems, Inc. recalls PTS Diagnostics CardioChek Plus Professional Analyzer, New analyzer, boxed, with carrying case, Reference Numbers 2700
Polymer Technology Systems recalls CardioChek Plus Professional Analyzers with specific serial numbers from November 2016 to October 2019 due to potential battery overheating if inserted incorrectly.
Polymer Technology SystemsDec 2, 2019 - UnratedDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Amantadine Hydrochloride Tablets, 100 mg, 100-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd.,
Jubilant Cadista recalls 100mg Amantadine Hydrochloride tablets due to foreign substance in some tablets. This is a prescription-only product with potential safety concerns.
Jubilant CadistaDec 2, 2019 - Lower riskDrug
AuroMedics Pharma LLC recalls Moxifloxacin Ophthalmic Solution USP, 0.5%, Sterile, 3mL Bottle, Rx Only, For Topical Ophthalmic Use Only, Distributed
AuroMedics recalls 0.5% Moxifloxacin eye drops due to discoloration complaints. Affected lots from India with specific expiration dates. Stop using if discoloration occurs.
AuroMedicsDec 2, 2019 - Stop using nowDrug
Preferred Pharmaceuticals, Inc recalls Ranitidine Tablets, USP 150 mg, OTC, a.) 30 count bottle (NDC 68788-7078-03), b.) 60 count bottle (NDC 68788-7078-06),
Preferred Pharmaceuticals recalls 150mg Ranitidine Tablets due to detected NDMA impurity. Consumers should stop using these products immediately.
Preferred PharmaceuticalsDec 2, 2019 - Stop using nowFood
ASK Foods Inc recalls Jonah Crab Meat Stuffing 5 lb. (2.27 kg) Bulk Plastic Container,6 - 5 lb. containers per case , Keep Frozen
ASK Foods recalls Jonah Crab Meat Stuffing 5 lb containers due to Listeria monocytogenes contamination. Consumers should stop using if frozen and thawed.
ASK FoodsDec 2, 2019 - Lower riskFood
Dole Fresh Vegetables Inc recalls Tri-Color Coleslaw - Marketside brand; 16 oz. plastic bag, SKU 3117 Colorful Coleslaw/Salade de Chou - President's
Dole recalls Tri-Color Coleslaw with green and red cabbage and carrots due to Salmonella contamination. Products sold in Canada with UPC 6-81131-38748-4 or 0-60383222670 from December 2019.
DoleDec 2, 2019 - Stop using nowFood
CornFusion Gourmet Popcorn, LLC recalls Caramel flavored Popcorn, packaged in poly lined bags, net wt. 7 oz. (198 g). No UPC code.
CornFusion Gourmet Popcorn recalls 12 packages of caramel popcorn due to undeclared milk. Check your pantry for this specific lot.
CornFusion Gourmet PopcornDec 2, 2019 - Use cautionMeat & poultry
Blue Grass Quality Meats Recalls Pork and Turkey Products due to Misbranding and Undeclared Allergens
USDA recalls 121,083 pounds of pork bacon and turkey products from Blue Grass Quality Meats due to soy allergen not declared on labels. Consumers urged not to consume these products.
Blue Grass Quality MeatsNov 29, 2019 - Stop using nowFood
Laubscher Cheese Company, Ltd. recalls Laubscher Cheese Co.; Shredded Cheese; Net Wt. 5 LBS. and 2 LBS.,Cryovac sealed plastic bags, Distributed By: Laubscher
Laubscher recalls shredded cheese products from October 2019 due to Listeria Monocytogenes contamination. Consumers should stop using these products immediately.
LaubscherNov 29, 2019 - Lower riskFood
Middlefield Original Cheese Coop recalls Shredded Parmesan Cheese Packaged in plastic 5lb bags, 4 bags per box
Middlefield Original Cheese Coop recalls shredded parmesan cheese packaged in 5lb plastic bags (4 per box) from Oct 9 to Nov 25, 2019, due to potential Listeria monocytogenes contamination.
Middlefield Original Cheese CoopNov 29, 2019 - Lower riskMedical device
AAP Implantate Ag recalls aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
AAP Implantate Ag recalls soft tissue retractors with lot numbers I012, I025, I028 due to potential debris retention after use. Affected medical devices may cause tissue damage if not properly removed during surgery.
AAP Implantate AgNov 28, 2019 - Use cautionVehicle
BMW Z4 (2020) recall — Exterior Lighting
BMW is recalling 2020 Z4 models for headlight control unit failure that can cause loss of headlights, increasing crash risk. Owners will receive free replacement units starting January 17, 2020.
BMWNov 27, 2019 - Use cautionMedical device
Edwards Lifesciences, LLC recalls QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705
Edwards Lifesciences recalls QuickDraw Venous Cannula models QD22 and QD25 due to risk of blood loss if used longer than 6 hours, especially during ECMO. Affected units have specific UDI numbers.
Edwards LifesciencesNov 27, 2019 - Use cautionMedical device
Flexicare Medical Ltd. recalls BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile
Flexicare recalls BriteBlade Pro laryngoscope blades due to risk of loose parts entering oral cavity during use, potentially delaying procedures. Affected units have specific part numbers and were sold with CE 0120 marking.
FlexicareNov 27, 2019 - Lower riskDrug
Pfizer Inc. recalls 25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA,
Pfizer recalls 25% Dextrose Injection (250 mg/mL) due to incorrect or missing expiration date on labels. This affects single-dose medical products sold to hospitals. Contact Pfizer for details.
PfizerNov 27, 2019 - Lower riskFood
Cell-nique Corp dba Living Harvest at Hudson River Foods recalls Hodgson Mill Unbleached All-Purpose White Wheat Flour 5 Lb bags 001042 Best By 10-01-2020 005517 Best By 10-02-2020
Living Harvest recalls Hodgson Mill Unbleached All-Purpose White Wheat Flour bags from 2020 due to potential STEC E. coli contamination. Consumers should check product codes and contact the company for details.
Living HarvestNov 27, 2019 - Lower riskFood
Skidmore Sales & Distributing Co Inc recalls CBI BG 2280/45025, 50 lb. package, 1 poly bag in cardboard box, 1140496
Skidmore recalls 50-lb soy lecithin packages with undeclared soy lecithin. Consumers should check product labels for lot numbers and contact Skidmore for details.
SkidmoreNov 27, 2019 - Stop using nowConsumer product
Stanley Black & Decker Recalls Wooden Handle Nailing Hammer Due to Injury Hazard
Stanley recalls 16 oz wooden handle nailing hammers with loose grip that may cause injury. Return to Walmart for gift card refund.
StanleyNov 27, 2019 - Use cautionVehicle
VOLVO S60 (2017) recall — Latches/Locks/Linkages
Volvo recalls 2011-2017 S60 models with faulty door latches that could open mid-drive, risking injury. Owners must have latches replaced free by dealers.
VolvoNov 26, 2019 - Use cautionVehicle
FOREST RIVER XLR (2020) recall — Tires
Forest River recalls 2020 XLR Boost trailers with undersized axles and tires that may cause trailer overload, increasing crash risk. Owners must contact customer service for free axle and tire repairs.
Forest RiverNov 26, 2019 - Use cautionMedical device
Deerfield Imaging, Inc. recalls iMRX MRI and Angiography System, part number 10094137 and 10094141, a surgical/interventional suite with integrated MRI
Deerfield Imaging recalls iMRX MRI and Angiography Systems with specific part numbers due to potential X-ray tube failure from generator A100 power supply issues. Affected units may not produce X-rays during procedures.
Deerfield ImagingNov 26, 2019
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