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
34,896 found- Use cautionMedical device
AESDEX recalls AesDex, LLC Cardica C-Port Flex-A PLUS Distal Anastomosis System, Catalog Number: FG-000150 The Cardica C-Port Flex-A
AESDEX recalls Cardica C-Port Flex-A PLUS Distal Anastomosis Systems due to potential handle damage and plastic fragments after pressurization, which could cause injury during medical procedures.
AESDEXApr 2, 2018 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented
Zimmer Biomet recalls hip implants with potentially mixed head sizes, risking dislocation during surgery. Affected patients should contact the company for details.
Zimmer BiometApr 2, 2018 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Bivona¿ Tracheostomy Tube Tracheostomy Tubes
Smiths Medical recalls tracheostomy tubes with non-sterile labeling. Devices sold as sterile but not actually sterile pose infection risks. Consumers should check model numbers and contact Smiths Medical for details.
Smiths MedicalApr 2, 2018 - Lower riskMedical device
Synthes (USA) Products LLC recalls Retractor f/Sciatic Nerve; Part number: 03.100.013; UDI: 10886982070623
Synthes recalls sciatic nerve retractors with part number 03.100.013 due to potential microspores forming in the handle that could allow fluid to enter. Affected units include specific lot numbers.
SynthesApr 2, 2018 - Lower riskDrug
Diamond Wipes International, Inc. recalls WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA
Diamond Wipes recalls 30-count WipeEssentials Wet Wipes with benzalkonium chloride 0.13% due to CGMP deviations in water quality. Affected lots expired by March 2018 and later. Consumers should check lot numbers on packaging.
Diamond WipesApr 2, 2018 - Stop using nowConsumer product
Polaris Recalls RZR XP 1000 Recreational Off-Highway Vehicles (ROVs) Due to Fire Hazard
Polaris recalls 2014-2018 RZR XP 1000 off-road vehicles due to fire risk from exhaust silencer cracks. Affected models have specific VIN and sticker markings. Contact dealer for free repair.
PolarisApr 2, 2018 - Use cautionVehicle
AUDI A6 (2011) recall — Air Bags
Audi is recalling 2011 A6 vehicles with passenger air bag inflators that may explode in crashes, causing serious injury or death. Owners must have the inflator replaced free of charge by dealers.
AudiApr 1, 2018 - Use cautionVehicle
GULF STREAM AMERILITE (2012) recall — Equipment
Gulf Stream recalls certain 2011-2012 recreational trailers with Kidde fire extinguishers that may become clogged or detach, increasing fire injury risk. Owners must contact Kidde for free replacement.
Gulf StreamApr 1, 2018 - Use cautionMeat & poultry
PFP Enterprises LLC Recalls Raw Beef Products Produced Without Benefit of Inspection
USDA FSIS recalls approximately 7,146 pounds of raw beef products made without federal inspection. Consumers are urged not to consume these items and should discard or return them.
PFP EnterprisesMar 31, 2018 - Lower riskFood
Club 13 Enterprises Warehouse recalls Club 13 Kratom Maeng Da Red XS capsules; 5, 20, 25, 40, 50 capsule bottles
Club 13 Enterprises Warehouse recalls Kratom capsules due to Salmonella contamination in samples. Affected products include 5, 20, 25, 40, and 50-count bottles with specific lot numbers.
Club 13Mar 31, 2018 - Use cautionVehicle
VAN HOOL CX35 (2017) recall — Seat Belts
Van Hool is recalling 2017 CX35 motorcoaches with exposed seat belt buckles that may increase crash injury risk. Owners must have defective buckles replaced by dealers.
Van HoolMar 30, 2018 - Use cautionMedical device
Edwards Lifesciences, LLC recalls Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in a sterile barrier system. Model Number:
Edwards Lifesciences recalls IntraClude Intra-Aortic Occlusion Devices with possible leak at distal open end causing medical staff to add inflation fluid. Affected units include specific model numbers and lot numbers.
Edwards LifesciencesMar 30, 2018 - Use cautionMedical device
PENTAX of America Inc recalls C2 CryoBalloon Focal Catheter, REF FG-1009. C2 CryoBalloon Ablation System is used as a cryosurgical tool in the field
Pentax recalls C2 CryoBalloon Focal Catheter (REF FG-1009) due to potential detachment from controller during surgery. Affected units have specific lot codes.
PentaxMar 30, 2018 - Use cautionMedical device
GE Medical Systems, LLC recalls MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic
GE Medical Systems recalls MR Surgical Option products with GE Signa 3.0T or 1.5T scanners due to potential patient transfer mechanism failure during surgery. Affected models include M8074SS, M8053SS, and others. Contact GE for remedy.
GE Medical SystemsMar 30, 2018 - Lower riskMedical device
Immuno-Mycologics, Inc recalls Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Model # CR2003 Product Usage: The CrAg Lateral Flow Assay is an
Immuno-Mycologics recalls Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Model CR2003 due to potential false negative results in cryptococcosis testing. Affected lots L102802 and L103012.
Immuno-MycologicsMar 30, 2018 - Stop using nowMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance 16 with DEPMED HARDENING KIT 12NC: 453567400741, Model Number 728240. Computed Tomography X-ray system
Philips recalls Brilliance 16 CT scanners with specific serial numbers due to risk of serious injury from patient support head holder contacting the back wall during motion. Affected units require immediate action to prevent permanent impairment.
Philips Medical SystemsMar 30, 2018 - Lower riskMedical device
Smith & Nephew, Inc. recalls smith&nephew LEGION(R) CR XLPE HIGH LEXION Articular Insert, 5-6 Size, 9 MM, REF 71453121 designed for use in patients
Smith & Nephew recalls specific articular inserts due to improper packaging that may cause injury during surgery. Affected products include batch numbers 11DM11664 and 15BM09445.
Smith & NephewMar 30, 2018 - Use cautionMedical device
Think Surgical, Inc. recalls Think Surgical Cutter, Flat, ¿6.2mm x 144mm. For use only with the TCAT Computer-Assisted Tool. Part Number 106428 The
Think Surgical recalls flat cutters (part 106428) for potential cutter head detachment. Affected units sold with TCAT tool; stop using if you own this specific model.
Think SurgicalMar 30, 2018 - Lower riskDrug
Marcas Usa Llc recalls PASTA DE LASSAR ANDROMACO Skin Protection, 25% zinc oxide Topical cream, 60 gram tube, UPC #851357003004, NDC
Marcas Usa recalls 60g zinc oxide skin cream with microbial contamination risk. Products with lot numbers 15PL041-17LP117 and expiration dates up to 10/20 may be unsafe.
Marcas UsaMar 30, 2018 - Lower riskDrug
AVKARE Inc. recalls Amantadine HCl Capsules, USP, 100 mg, 50 Capsules (5x10) Unite Dose, Rx Only, Manufactured for: AvKARE Inc. Pulaski, TN
AVKARE recalls 100 mg Amantadine HCl Capsules (NDC 50268-069-15) due to failed dissolution specifications. This may affect medication effectiveness. Check your product details to determine if you are affected.
AVKAREMar 30, 2018 - Use cautionFood
Taylor Shellfish Co recalls Original Smoked Oysters, packaged in vacuum pouches, net wt. 2.25 oz. or 16 oz.. UPC 47094 20002
Taylor Shellfish Co recalls Original Smoked Oysters in vacuum pouches (2.25 oz or 16 oz) because improper packaging risks botulism. Products may cause food poisoning if kept above 38°F.
Taylor Shellfish CoMar 30, 2018 - Use cautionFood
Funky Chunky LLC recalls funky chunky Chocolate Pretzels. Pretzels, Caramel, Chocolate, Pecans. Sold in the following packaging configurations:
Funky Chunky recalls chocolate pretzels that may contain undeclared tree nuts and peanuts due to shared facility risks. Check packaging for UPCs 91056-00045, 91056-00040, 91056-00084, etc. to see if your product is affected.
Funky ChunkyMar 30, 2018 - Stop using nowFood
Nutrizone LLC recalls Cali Thai Kratom all packages, all quantities
Nutrizone recalls all Cali Thai Kratom products due to potential Salmonella contamination in dietary supplements. Consumers should stop using affected items immediately.
NutrizoneMar 30, 2018 - Lower riskFood
AdvoCare International, LP recalls AdvoCare Muscle Strength Dietary Supplement with HMB and Suma Product code, P3221
AdvoCare recalls Muscle Strength dietary supplement with HMB and Suma due to undeclared milk. This may cause allergic reactions in sensitive individuals. Stop using immediately.
AdvoCareMar 30, 2018 - Use cautionMeat & poultry
Target Corporation Recalls Frozen Ready-To-Eat and Non-Ready-To-Eat Meat and Poultry Products due to Possible Temperature Abuse During Transport at a Single Store on Oahu, Honolulu, HI
Target recalls frozen meat and poultry products from March 23-27, 2018 that may have been exposed to unsafe temperatures during transport, risking growth of harmful bacteria.
TargetMar 29, 2018 - Use cautionVehicle
TESLA MODEL S (2014) recall — Steering
Tesla is recalling 2012-2016 Model S vehicles with Bosch steering racks due to risk of power steering loss, which could increase crash risk at low speeds. Owners must contact Tesla for free repair.
TeslaMar 29, 2018 - Use cautionVehicle
ALFA ROMEO STELVIO (2018) recall — Structure
Chrysler recalls 2018 Alfa Romeo Stelvio vehicles with potential liftgate corrosion causing unintended opening at low speeds, risking cargo falls and crashes. Owners must contact Chrysler for free repair.
Alfa RomeoMar 29, 2018 - Use cautionVehicle
ALFA ROMEO STELVIO (2018) recall — Equipment
Chrysler recalls 2018 Alfa Romeo Stelvio vehicles with water leaks into the body control module causing wiper and light malfunctions. Owners must contact Chrysler for a fix by April 25, 2018.
Alfa RomeoMar 29, 2018 - Use cautionVehicle
INTERNATIONAL LT (2019) recall — Fuel System, Diesel
Navistar recalls 2018-2019 International LT trucks with potential fuel leaks causing fire or crash risks. Owners must get a free repair to prevent leaks.
NavistarMar 29, 2018 - Lower riskMedical device
Brewer Company, LLC recalls Access Hi-Low Exam Tables, Model 6501-XX
Brewer recalls Access Hi-Low Exam Tables Model 6501-XX with over-crimped wire harness that may cause electrical issues. Affected units include specific lot numbers from HL018786 to HL018805.
BrewerMar 29, 2018
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83,392 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.