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
34,894 found- Lower riskMedical device
Becton Dickinson & Co. recalls BD MAX DNA MMK (SPC) For Laboratory Use, catalog no. 442829
Becton Dickinson recalls BD MAX DNA MMK (SPC) lab reagents from August 2014 due to incorrect primer/probe diluent volume in package inserts, potentially affecting assay results.
Becton DickinsonMar 2, 2018 - Lower riskMedical device
Randox Laboratories Ltd. recalls Lipase, Catalog number: LI3837; GTIN: 05055273204230 and Catalog number: LI8361; GTIN: 05055273214284 Product Usage:
Randox recalls two lipase test kits (LI3837 and LI8361) for potential contamination in lab testing of pancreatic diseases. Affected kits may cause inaccurate results if used on medical devices.
RandoxMar 2, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls BECKMAN COULTER iQ200 Series Urine Microscopy Analyzer, Catalog Numbers: 700-3345, C10684, 700-3375, C10683, 700-3325,
Beckman Coulter recalls iQ200 Series Urine Microscopy Analyzers with specific catalog numbers due to potential under-reporting of casts in urine tests. Affected units may require software reconfiguration to prevent inaccurate results.
Beckman CoulterMar 2, 2018 - Use cautionMedical device
Getinge Disinfection Ab recalls Getinge AGS, FSLC, FSUC, RC accessory to Washer- Disinfector 86 Series UDI Info: 86 Series Washer Disinfector
Getinge recalls accessories for 86 Series Washer Disinfector models due to potential cart unloading without trolley docking, risking falls and damage. Affected units have specific serial numbers.
GetingeMar 2, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls BECKMAN COULTER iChemVELOCITY, Urine Chemistry System, Catalog Numbers: 800-3530, 800-7167, 800-7719, 800-7720, 800-
Beckman Coulter recalls North American iChemVELOCITY Urine Chemistry Analyzers with potential for incorrect settings causing false low results. Affected units include specific catalog numbers and configurations.
Beckman CoulterMar 2, 2018 - UnratedDrug
Renaissance Lakewood, LLC recalls Flucanazole Injection, USP 200 mg in in 100 mL (2 mg/mL), 10 Single Dose Flexible Containers, Rx Only, Manufactured
Renaissance Lakewood recalls Flucanazole Injection due to stability problems that could affect drug potency and safety. This medication is prescription-only and sold in specific packaging.
Renaissance LakewoodMar 2, 2018 - Stop using nowFood
RIPPLE FOODS PBC recalls ripple Chocolate Nutritious Pea Milk; 48 oz. plastic bottle; 8 g Plant Based Protein 30% Less Sugar than Chocolate
Ripple Foods recalls 48oz chocolate pea milk due to high coliforms and Serratia liquefaciens bacteria. Consumers should stop using affected products immediately.
Ripple FoodsMar 2, 2018 - Lower riskMeat & poultry
Sensenig Turkey Farm LLC Recalls Turkey Sausage Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 1,925 pounds of Sensenig Turkey Farm turkey sausage products due to undeclared wheat and soy allergens. Consumers are urged not to consume these products.
Sensenig Turkey FarmMar 1, 2018 - Use cautionMeat & poultry
J Bar B Foods Recalls Chicken Sausage Products due to Misbranding and an Undeclared Allergen
USDA FSIS recalls 4,050 pounds of chicken sausage products due to undeclared milk allergen and misbranding. Consumers urged not to consume and dispose of recalled items.
J Bar B FoodsMar 1, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls VIDAS LH, Reference Numbers 30406 and 30406-01. Poduct Usage: VIDAS LH is an automated quantitative test for use on the
BioMérieux recalls VIDAS LH tests with reference numbers 30406 and 30406-01 due to calibration problems using low calibrator S1. Affected lots may show decreased strip signals over time.
BioMérieuxMar 1, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size 4
Zimmer recalls certain hip implants that contain a smaller size than labeled, which could lead to improper fit and complications. Affected packages have specific part and lot numbers.
ZimmerMar 1, 2018 - Use cautionMedical device
Draeger Medical, Inc. recalls Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for
Draeger Medical recalls Fabius MRI anesthesia machines (serial numbers ASKM-0020, ASKM-0011, etc.) due to potential ventilation failure if motor position detection is disturbed or cover is damaged. This could affect patient safety during surgery.
Draeger MedicalMar 1, 2018 - Use cautionMedical device
ICU Medical de Mexico, S.A. de C.V. recalls 38 cm (15") Smallbore Ext Set w/6-Port NanoClave Manifold, Check Valve, MicroClave Clear, 3 Gang 4-Way NanoClave
ICU Medical recalls 38cm IV sets with NanoClave manifold due to potential leaks or separation between components. Affected units have specific lot numbers and expiration dates.
ICU MedicalMar 1, 2018 - Lower riskFood
Gilster-Mary Lee Corp. recalls Food Club, Essential Choice, Puffed Rice, Net Wt 6 Oz (170 g), UPC 36800 31852
Gilster-Mary Lee recalls 6oz puffed rice cereal due to undeclared wheat allergen on packaging. Consumers should check UPC 36800 31852 for affected products.
Gilster-Mary LeeMar 1, 2018 - Lower riskFood
WEIS MARKETS recalls Dried Beef Party Rye Dip; Ingredients: Hellman's Mayonaise, Sour Cream, Dried Beef (Cured with Water, Salt, Sugar,
Weis Markets is recalling Dried Beef Party Rye Dip due to undeclared egg and milk in the product. This recall affects products sold with specific sell-by dates and may pose a risk for individuals with allergies.
Weis MarketsMar 1, 2018 - Lower riskFood
KUIYI INTERNATIONAL INC. recalls XZB Grilled Crispy Shrimp (20g*20 and 16g*24) UPC Code (16g) 6923006800082
KUIYI International recalls Grilled Crispy Shrimp (20g*20 and 16g*24) with UPC 6923006800082 due to nitrofurans detected. Consumers should check expiration date and stop using if concerned.
KUIYIMar 1, 2018 - Use cautionConsumer product
Graco Recalls Highchairs Due to Fall Hazard; Sold Exclusively at Walmart
Graco recalls 6-in-1 highchairs with model 1969721 due to rear leg instability causing fall hazards. Consumers must stop using and get a free repair kit from Graco.
GracoMar 1, 2018 - Use cautionConsumer product
Goodman Company Recalls Packaged Terminal Air Conditioners and Heat Pumps Due to Burn and Fire Hazards
Goodman recalls beige Packaged Terminal Air Conditioners and Heat Pumps with specific model numbers and serial ranges due to outdoor fan motor overheating risks.
GoodmanMar 1, 2018 - Stop using nowConsumer product
Double Insight Recalls Multicookers Due to Fire Hazard; Sold Exclusively at Walmart
Gem 65 8-in-1 multicookers with batch codes 1728, 1730, 1731, 1734 or 1746 have a fire hazard due to overheating. Recalled units sold exclusively at Walmart require immediate stop use and return for free replacement.
GemMar 1, 2018 - Lower riskMedical device
Biomet, Inc. recalls Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic implants for Proximal Humeral Reconstruction,
Biomet recalls specific orthopedic implants for humeral reconstruction due to assembly failure risk. The mismatched screw holes may prevent proper screw engagement during surgery in less than 1% of cases.
BiometFeb 28, 2018 - Lower riskMedical device
Vygon U.S.A. recalls PICC Tray, Product Code: AMS-9093CP Convenience kit for the insertion of PICCs into the vascular system.
Vygon recalls PICC Tray (AMS-9093CP) with lot numbers 16I026D and 16J032D due to potential friction holes that could compromise sterility. Affected users should contact Vygon for details.
VygonFeb 28, 2018 - Lower riskMedical device
Zimmer GmbH recalls Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496
Zimmer recalls Avenir Muller Stem (Lot 2905496) due to potential mismatch between product in package and outer label. Consumers should check labels and contact Zimmer for details.
ZimmerFeb 28, 2018 - Lower riskDrug
Osmotica Pharmaceutical Corp recalls Methylphenidate Hydrochloride Extended-release Tablets, USP, 36 mg, 100-count bottle, Rx only, Trigen Laboratories, LLC
Osmotica recalls 36mg Methylphenidate ER tablets due to subpotent drug content. Affected lots: 170231B-170234A. Consumers should contact pharmacy for replacement.
OsmoticaFeb 28, 2018 - Stop using nowFood
Blue Moose of Boulder, LLC recalls All-Natural Ciolo Nut-Free Basil Pesto, 7 oz., plastic container, Item #: 30019.18
Blue Moose of Boulder recalls Ciolo Nut-Free Basil Pesto due to undeclared tree nuts. Check your pantry for lot BV431291.
CioloFeb 28, 2018 - Lower riskFood
Adams Extract & Spice LLC recalls Adams Reserve, Fajita Grilling Rub 5.7 oz. Bottle Item Code: 04544, 12 bottles per case
Adams Recall: Fajita Grilling Rub 5.7oz bottles with item code 04544 contain undeclared wheat. Consumers should check product labels for affected items.
AdamsFeb 28, 2018 - Lower riskFood
ASR GROUP INTERNATIONAL INC recalls Tank Truck #2 Sugar Syrup (403764)
ASR Group International recalls Tank Truck #2 Sugar Syrup (lot 18092 or : foreign metal in product. Not all affected units; check labels for lot numbers.
ASR Group InternationalFeb 28, 2018 - Use cautionConsumer product
PL Sleep Children's Sleepwear Recalled by Lemur Group Due to Violation of Federal Flammability Standard
PL Sleep recalls children's nightgowns that fail flammability standards, risking burns. Return to retailer or contact for refund.
PL SleepFeb 28, 2018 - Stop using nowVehicle
HYUNDAI SONATA (2013) recall — Seat Belts
Hyundai recalls 2011-2013 Sonata vehicles due to a short circuit in the air bag control unit that may prevent safety systems from deploying in a crash.
HyundaiFeb 27, 2018 - Use cautionMedical device
Iridex Corporation recalls Iridex TruFocus LIO Premiere" Laser Indirect Ophthalmoscope ( LIO ) The LIO is a headmounted indirect ophthalmoscope
Iridex recalls TruFocus LIO Premiere laser ophthalmoscopes due to risk of focal cataracts and iris burns from improper laser energy delivery. Affected models include 87300-87304.
IridexFeb 27, 2018 - Lower riskMedical device
Integrity Implants Inc. recalls FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product
Integrity Implants recalls FlareHawk Interbody Fusion System Instructions for Use (IFU's) due to potential cleaning parameter discrepancies in labeling. Affected users should verify their IFU version and contact the company for updates.
Integrity ImplantsFeb 27, 2018
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