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- Stop using nowFood
Tai Foong USA Inc recalls Costco item # 1052939, Royal Asia brand Shrimp Wonton Noodle Soup, 6 bowls per case. Net weight 3.94lb (1.79kg) 63oz.
Costco's Royal Asia Shrimp Wonton Noodle Soup (6 bowls) recalled due to undeclared egg. Check UPC 877971005361 for affected items.
Royal AsiaSep 29, 2017 - Lower riskFood
Dean Foods, Inc. recalls Tampico Tropical Punch packaged in 1 gallon plastic jugs
Dean Foods recalls Tamp: 1-gallon plastic jugs with BEST BY date 12/27/2017 due to undeclared milk in fruit punch. Consumers should check UPC 095188031281.
Dean FoodsSep 29, 2017 - Lower riskFood
Beyond Better Foods Llc recalls ENLIGHTENED THE GOOD-FOR-YOU ICE CREAM 60 CALORIES PER SERVING PINA COLADA MORE PROTEIN. LESS SUGAR 1 PINT LOW FAT ICE
Beyond recalls Enlightened Piña Colada Ice Cream due to undeclared coconut. Consumers should check UPC 8 52109 33108 6 for affected products.
BeyondSep 29, 2017 - Stop using nowFood
Pinnacle Food Group, Llc recalls Birds Eye Baby Sweet Peas, Net Wt. 13 oz. (369g ), Keep Frozen. UPC 14500-02253.
Birds Eye Baby Sweet Peas (13 oz) recalled due to potential Listeria monocytogenes contamination. Check your freezer for specific lot numbers.
Birds EyeSep 29, 2017 - Stop using nowFood
Greencore USA, LLC recalls Hannaford Ham Salad Club Roll, 5.1 oz
Greencore USA recalls Hannaford Ham Salad Club Rolls (5.1 oz) due to possible Listeria monocytogenes contamination. Check your fridge.
HannafordSep 29, 2017 - Use cautionVehicle
BMW X3 (2010) recall — Air Bags
BMW is recalling certain 2006-2010 X3 models due to potential front passenger air bag failure in crashes, increasing injury risk. Owners must have the seat occupant detection mat replaced free of charge.
BMWSep 28, 2017 - Lower riskMedical device
Philips Electronics North America Corporation recalls Automated External Defibrillator - HeartStart MRx Monitor/Defibrillator
Philips recalls 20 units of HeartStart MRx defibrillators due to potential EtCO2 module contamination causing inaccurate CO2 waveform displays. Affected units have specific serial numbers listed in the recall.
PhilipsSep 28, 2017 - Use cautionMedical device
Sorin Group USA, Inc. recalls FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is
Sorin Group recalls FlexFlow Venous Cannula Model 200-200 due to sharper tip than expected. This may cause injury during medical procedures. Affected units have specific lot numbers.
Sorin GroupSep 28, 2017 - Use cautionMedical device
Tosoh Bioscience Inc recalls AIA-900 Automated Immunoassay Analyzer performs three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich
Tosoh recalls AIA-900 analyzers with potential harness wear causing system errors. Affected units may show error code 4093 and stop functioning. No injuries reported.
TosohSep 28, 2017 - Lower riskMedical device
Steris Corporation recalls V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)
Steris recalls V-PRO 60 Low Temperature Sterilization System with serial numbers listed; update software to prevent using expired sterilant before sterilization cycles start.
SterisSep 28, 2017 - Lower riskMedical device
The Magstim Company Limited recalls Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air
Magstim recalls 4800-0:0T Rapid Therapy System units due to missing user manuals. This could affect safe use of the device for treating depression.
MagstimSep 28, 2017 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless foot switch accessory; Model Numbers:
Siemens recalls Artis Q and Q.zen model Interventional fluoroscopic x-ray systems wireless foot switches due to potential failure from electrostatic discharge, which could prevent radiation release during procedures. Affected units have specific model and serial numbers listed.
Siemens Medical SolutionsSep 28, 2017 - Use cautionMedical device
Cosmedent, Inc. recalls Cosmedent's Etching Gel, 3g, 37% Phosphoric Acid, Rx only. Packaged in 3g Luer Lock syringes. Used for etching enamel
Cosmedent recalls 3g Etching Gel with non-Luer Lock syringes that may detach during use, posing a risk of injury. Affected units include SKU #663-103, Lot 164222A, expiring 10/31/2019.
CosmedentSep 28, 2017 - Lower riskDrug
Leading Pharma, LLC recalls Lorazepam Tablets, USP CIV, 0.5 mg, 500-count bottle, Rx Only, Manufactured by: Leading Pharma, LLC Fairfield, NJ 07004
Leading Pharma recalls 500-count lorazepam tablets labeled 0.5mg but contain 1mg. This labeling error may cause incorrect dosing. Consumers should contact the company for details.
Leading PharmaSep 28, 2017 - Stop using nowFood
Hong Lee Trading recalls VINA CAF¿ WAKE-UP INSTANT COFFEE MIX in 18 PACK CARDBOARD BOXES (.6 oz packs); UPC: 8 934683 002759
Hong Lee Trading recalls Vina Cafe Wake-Up Instant Coffee Mix due to undeclared milk. Check your UPC and expiration date for details.
Vina CafeSep 28, 2017 - Lower riskFood
Ricker Hill Farms recalls (1) Ricker Hill Orchards Apple Cider packaged in plastic Half Gallon UV Treated (64 fl. oz.) Jugs UPC 7461380009 (2)
Ricker Hill Farms recalls two apple cider products due to patulin levels above FDA's 50ppb limit. Consumers should avoid these items to prevent potential health risks.
Ricker Hill FarmsSep 28, 2017 - Stop using nowConsumer product
Skip Hop Recalls Nightlight Soothers Due to Shock Hazard
Skip Hop recalls Moonlight & Melodies nightlight soothers due to risk of electrical shock from faulty USB wall power adapters. Consumers must stop using and return the adapter for free repair.
Skip HopSep 28, 2017 - Stop using nowMeat & poultry
America New York RI Wang Food Group Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
America New York RI Wang Food Group recalls approx. 63,823 lbs of beef and pork sausage products due to undeclared milk allergen. Do not consume.
America New York RI Wang Food GroupSep 27, 2017 - Use cautionVehicle
FORD EDGE (2010) recall — Suspension
Bearing Technologies recalls certain 2007-2010 Ford Edge wheel spindles with oversized shoulder studs that may cause wheel vibration or wobble, increasing crash risk. Owners can get free repairs.
BearingSep 27, 2017 - Use cautionMedical device
WalkMed, LLC recalls Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed
WalkMed recalls 65mL and 150mL reservoir bags for infusion pumps due to reported fluid leaks at luer connections. Affected units may cause leaks near the clear female luer connector.
WalkMedSep 27, 2017 - UnratedDrug
Pfizer Manufacturing Deutschland GmbH recalls FOR EXPORT ONLY Atorvastatin calcium Film-Coated Tablets a) 80 mg SMT Tabs Bulk, b) 40 mg SMT G EP PR KR, c) 20 mg SMT
Pfizer recalls specific batches of atorvastatin calcium tablets for export due to microbial contamination in non-sterile products. This could pose a risk of infection if used.
PfizerSep 27, 2017 - Stop using nowDrug
United Pharmacy recalls Glutamine, Arginine and Carnitine, 10/100/200mg/mL, 30 mL (Multi Dose Vial), Rx Only, For Injection, United Pharmacy
United Pharmacy recalls 268 vials of Glutamine, Arginine and Carnitine injection due to CGMP deviations. Check your lot numbers for safety.
United PharmacySep 27, 2017 - Stop using nowConsumer product
DICK'S Sporting Goods Recalls Resistance Tubes Due to Injury Hazard
DICK's Sporting Goods recalls fitness resistance tubes that can break during use and cause injury. Return to store for refund or credit.
DICK's Sporting GoodsSep 27, 2017 - Use cautionVehicle
RAM PROMASTER CITY (2017) recall — Equipment
Chrysler recalls 2015-2017 RAM ProMaster City vehicles with incorrect tire placards that may cause unsafe weight or tire pressure, increasing crash risk. Owners must get corrected placards free.
ChryslerSep 26, 2017 - Use cautionMedical device
Medtronic Inc recalls 6F Taiga Guiding Catheter
Medtronic recalls 6F Taiga Guiding Catheter with specific lot/serial numbers due to complaints of tip detachment and splitting. Affected users should check their device details.
MedtronicSep 26, 2017 - Use cautionMedical device
Mobius Imaging, LLC recalls AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed
Mobius Imaging recalls AIRO Mobile CT System Model MobiCT-32 due to risk of unintended motion during startup. Affected units may cause injury if the tilt-drive motor has a connection issue or broken sensor wire.
Mobius ImagingSep 26, 2017 - Use cautionMedical device
Integra LifeSciences Corp. recalls Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System; Catalogue No: C7000 Product Usage: The
Integra LifeSciences recalls Footswitch (C7000) for CUSA Clarity system due to risk of unintended ultrasonic tissue fragmentation during surgery. Affected units include specific lots.
Integra LifeSciencesSep 26, 2017 - UnratedDrug
The Harvard Drug Group recalls Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma
Harvard Drug Group recalls 0.25mg Alprazolam tablets with unknown impurity. Consumers should contact the manufacturer for details on affected lots.
The Harvard Drug GroupSep 26, 2017 - Lower riskDrug
Pharmedium Services, LLC recalls morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by:
PharMEDium Services LLC recalls morphine sulfate injections with missing lot or expiration dates. Patients should contact their pharmacy for safe alternatives.
PharMEDiumSep 26, 2017 - UnratedDrug
Pharmedium Services, LLC recalls Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in 0.9% Sodium Chloride 10 mL syringes, PharMEDium Services, LLC 913 N
PharMEDium Services recalls phenylephrine HCl 100 mcg/mL syringes due to superpotent drug risk. Affected units have NDC 71019-263-20 and lot 172560019M.
PharMEDiumSep 26, 2017
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