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
34,893 found- Lower riskDrug
Premier Pharmacy Labs Inc recalls Neostigmine Methylsulfate (single dose syringe) 1 mg per mL 5 mg per 5 mL Injectable Hospital/Office Use Only
Premier Pharmacy Labs recalls neostigmine methylsulfate syringes due to labeling error indicating an expiry date beyond stability data. Affected lots have a 2018 expiry but may degrade faster than labeled.
Premier Pharmacy LabsAug 10, 2017 - Lower riskDrug
SSM Health Care St. Louis DBA SSM St. Clare Health Center recalls Norepinephrine 8 mg in dextrose 5% 250 mL, 250mL IV Bag, Concentration: 0.032 mg/mL, This is a compounded injectable
SSM St. Clare Health Center recalls specific norepinephrine IV bags (NDC 88890-0334-01) due to microbial growth detected in manufacturing simulations. No actual contaminated batches were found, but the risk requires immediate action.
SSM St. Clare Health CenterAug 10, 2017 - Lower riskFood
Zydot Unlimited, Inc recalls Zydot Ultimate Blend Detox Drink Natural Tropical Ice Flavor 32 fl. oz. (946 ml) and 16 fl. oz. (473 ml) packaged in
Zydot recalls Tropical Ice flavor detox drinks due to undeclared yellow #5 dye. Check product labels for lot 071017LT or UPC 5451528140.
ZydotAug 10, 2017 - Use cautionFood
Lakeside Foods, Inc recalls IQF Green Beans, Keep Frozen. 11 varieties, packaged under the following brands and sizes: 1) Bountiful Harvest French
Lakeside Foods recalls 11 varieties of frozen green beans packaged under brands like Bountiful Harvest and Sysco due to potential Listeria monocytogenes contamination. Consumers should check product codes and discard affected items.
Lakeside FoodsAug 10, 2017 - Stop using nowConsumer product
Kawasaki Recalls All-Terrain Vehicles Due to Fire Hazard
Kawasaki recalls 2012-2017 KFX50 and KFX90 ATVs due to fuel tap leaks that could cause fire. Affected models have specific VIN ranges and are sold in various colors.
KawasakiAug 10, 2017 - Lower riskMeat & poultry
Corn Maiden Foods, Inc. Recalls Ready-to-Eat Beef Products Due To Misbranding
Corn Maiden Foods recalls 2,133 pounds of ready-to-eat beef products due to misbranding: MSG not listed on labels. Products sold in California from Feb 2017 to March 2017.
Corn Maiden FoodsAug 9, 2017 - Use cautionMeat & poultry
Kenosha Beef International, LTD. Recalls Beef Products Due To Misbranding and Undeclared Allergens
USDA FSIS recalls 3,960 lbs of beef patties with undeclared milk and bacon due to misbranding. Consumers urged to stop using these products immediately.
Kenosha BeefAug 9, 2017 - Use cautionVehicle
GILLIG LOW FLOOR (2016) recall — Steering
Gillig recalls certain 2013-2016 Hybrid and Electric Low Floor buses due to potential loss of power steering assist, increasing crash risk. Owners must have steering motor-pump assemblies replaced free by dealers.
GilligAug 9, 2017 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris Pump Module model 8100 manufactured between November 2011 and March 2012; Alaris Pump Module serviced with LVP
CareFusion 303, Inc. - 13617430
CareFusion 303, Inc.Aug 9, 2017 - Lower riskMedical device
Medtronic Neuromodulation recalls Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The
Medtronic is recalling Synchromed II Model 8637 pumps with 20mL and 40mL reservoirs that may experience motor stall from corrosion. These devices are not implanted and require replacement.
MedtronicAug 9, 2017 - Use cautionFood
The Best Bar Ever Inc. recalls The Best Bar Ever, Peanut Butter Crunch, 1.41 oz., 40 gm.
The Best Bar Ever recalls Peanut Butter Crunch bars (40g) due to a mistaken gluten-free logo on the wrapper. Check your UPC and lot codes.
The Best Bar EverAug 9, 2017 - Lower riskFood
Ito En (USA) Inc. recalls Royal Mills, Iced Cappuccino, Premium Coffee. 11.0 FL. OZ. (325 ml) 2-piece aluminum can; Made in Hawaii. UPC: 0 73366
Ito En recalls Royal Mills Iced Cappuccino (11 fl oz cans) due to sour taste, off odor, and sediment in one lot. Consumers should check UPC 073366 for affected products.
Ito EnAug 9, 2017 - Stop using nowVehicle
BMW M6 (2013) recall — Air Bags
BMW is recalling 2013 M6 models with driver air bags that may separate during crashes, risking serious injury or death. Owners must replace the air bag module free of charge.
BMWAug 8, 2017 - Use cautionVehicle
DODGE CHALLENGER (2017) recall — Engine And Engine Cooling
Chrysler recalls 2017 Dodge Challengers with Hellcat engines due to potential oil leaks that could impair visibility and cause crashes or fires. Owners must have EOC lines replaced at no cost.
ChryslerAug 8, 2017 - Lower riskMedical device
Randox Laboratories, Limited recalls Liquid Cardiac Control CQ5053
Randox recalls Liquid Cardiac Control CQ5053 lot 4069CK due to shelf-life issues. The control may fall outside specified ranges, affecting accuracy.
RandoxAug 8, 2017 - UnratedMedical device
Alcon Research, LTD. recalls Alcon Custom Pak
Alcon recalls Custom Pak devices with specific model numbers due to supplier's x-ray detectable sponges. Affected units may pose risks during medical imaging procedures.
AlconAug 8, 2017 - Lower riskMedical device
LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC recalls REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue
LifeCell recalls REVOLVE Advanced Adipose System due to potential bacterial endotoxins above safe levels. Affected units have specific lot numbers with expiration dates through 2019. Consumers should check their product details.
LifeCellAug 8, 2017 - Use cautionMedical device
Leonhard Lang Medizintechnik GmbH recalls Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for
Leonhard Lang recalls specific lots of Skintact Electrodes DF59N and DF59NC that may not connect with ZOLL AED Plus defibrillators, risking delayed life-saving treatment for cardiac emergencies.
Leonhard LangAug 8, 2017 - Lower riskFood
Wegmans Food Markets, Inc. recalls Wegmans Apple Crostata, Large, Net Wt. 23 oz. and 6 oz. (In-Store Bakery)
Wegmans recalls large and small apple crostata products due to undeclared soy lecithin. Consumers should check product dates and contact Wegmans for details.
WegmansAug 8, 2017 - Stop using nowConsumer product
Polaris Recalls Scrambler All-Terrain Vehicles Due to Crash Hazard
Polaris recalls 2014-2017 Scrambler XP 1000 ATVs due to throttle switch failure risk. Stop using immediately and contact for free repair.
PolarisAug 8, 2017 - Stop using nowConsumer product
NVIDIA Recalls European Plug Heads Sold with Power Adaptors Due to Electric Shock Hazard
NVIDIA recalls European plug heads for SHIELD power adaptors due to risk of electric shock from broken prongs. Affected units include those sold in Europe with SHIELD tablet computers and TVs.
NVIDIAAug 8, 2017 - Stop using nowConsumer product
Meijer Recalls Children's Swimsuits Due to Choking Hazard
Meijer recalls Wave Zone children's swimsuits with detachable snaps that pose a choking hazard to young children. Return to any Meijer store for a full refund.
Wave ZoneAug 8, 2017 - Stop using nowMeat & poultry
Good Food Concepts, LLC. Recalls Beef Products Due To Possible E. Coli O26 Contamination
Good Food Concepts recalls approximately 1,290 pounds of raw beef products with lot codes 170731CC or 170803/170804 due to possible E. coli O26 contamination. Consumers are urged not to consume these products.
Good Food ConceptsAug 7, 2017 - Use cautionMedical device
Synthes, Inc. recalls LCP Drill Sleeve 1.5 Drill Bit 1.1mm Part Number 03.114.001 Used in LCP Modular Mini Fragment System, for fixation of
Synthes recalls LCP Drill Sleeve 1.5 Drill Bit 1.1mm Part Number 03.114.001 for possible surgical delay if drill sleeve doesn't attach properly to bone plates.
SynthesAug 7, 2017 - Stop using nowMedical device
Covidien LLC recalls Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1
Covidien recalls Emprint Percutaneous Antenna with Thermosphere Technology due to risk of ceramic tip disengaging post-ablation, potentially remaining in patient. Affected units have specific lot codes and UDI.
CovidienAug 7, 2017 - Lower riskMedical device
Microvention, Inc. recalls MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1 guidewire per package,
Microvention recalls Traxcess 7 Mini Guidewires with hydrophilic coating that may delaminate. Affected units have specific lot numbers. Contact for remedy.
MicroventionAug 7, 2017 - UnratedMedical device
Mako Surgical Corporation recalls Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is
Mako Surgical recalls Robotic Arm Interactive Orthopedic System (RIO) due to software not displaying all EE constants when screen is full. Affected units may have incomplete surgical guidance.
Mako SurgicalAug 7, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Persona Stemmed Tibial Provisional Size H Right, Item Number 42532108302 For use during orthopaedic surgery for
Zimmer Biomet recalls Persona Stemmed Tibial Provisional Size H Right devices due to potential cracks in raw materials that could compromise cleanliness during orthopedic surgery.
Zimmer BiometAug 7, 2017 - Use cautionMedical device
Spectranetics Corporation recalls Spectranetics Bridge Occlusion Balloon catheter, Sheath Compatibility 12F, Guidewire Compatibility 0.035in, Working
Spectranetics recalls specific Bridge Occlusion Balloon catheters due to potential guidewire passage issues, risking treatment delays in emergency procedures.
SpectraneticsAug 7, 2017 - Lower riskMedical device
Merge Healthcare, Inc. recalls Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare,
Merge Healthcare recalls specific software versions that may misidentify patients with atypical hyperplasia, leading to incorrect cancer risk assessments. Affected users must verify their software version and license status.
Merge HealthcareAug 7, 2017
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