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
Baxter Healthcare Corporation recalls MARS Treatment Kit, Use only with MARS(R) Monitor 1TC, GAMBRO, Product Code 800541
Baxter recalls MARS Treatment Kit (Product Code 800541) due to albumin circuit leakage from tubing connections. Affected units have specific lot numbers and were sold with MARS Monitor 1TC.
BaxterDec 21, 2017 - Use cautionMedical device
W & H DentalWerk Burmoos GMBH - Site 1 recalls Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot control for use with drive units operating mechanical
W & H DentalWerk recalls foot controls S-N1 and S-N2 models due to potential malfunction causing motor to keep rotating during procedures, risking serious patient injury. Affected units have specific serial numbers and were sold in certain regions.
W & H DentalWerkDec 21, 2017 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls (1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP
DePuy recalls specific Sigma HP cemented trochlear implants due to higher-than-expected revision rates observed in post-market use. Affected products include left and right narrow sizes 1-5 with catalog numbers 102403100-102404500.
DePuyDec 21, 2017 - Lower riskDrug
Taro Pharmaceuticals U.S.A., Inc. recalls Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay,
Taro Pharmaceuticals recalls 0.05% Clobetasol Propionate Cream tubes due to failed content uniformity. This may affect medication accuracy. Check your product details to see if you are affected.
TaroDec 21, 2017 - Stop using nowFood
Casper's Ice Cream, Inc recalls Red Button Vintage Creamery, Caramel Cashew Ice Cream, 56 fluid ounce. UPC 077865010109. Case Pack UPC # 077865010109
Red Button Vintage Creamery recalls 56 oz Caramel Cashew Ice Cream due to undeclared almonds. Check your UPC and lot number for details.
Red Button Vintage CreameryDec 21, 2017 - Lower riskFood
Nutricia North America recalls SHS Wel-Plan Wheat and Corn Strach Baking Mix , 400 g box,Cardboard carton, 18 cartons per case, but distributed by
Nutricia recalls SHS Wel-Plan Wheat and Corn Baking Mix due to low Klebsiella pneumonia contamination. The product is intended to be cooked, but some consumers may misuse it without cooking, creating a potential health risk.
NutriciaDec 21, 2017 - Lower riskFood
Saputo Cheese USA Inc. recalls Light String Cheese, Part Skim Mozzarella cheese, sold under the following brands and package sizes: 1. Fit & Active,
Saputo recalls Light String Cheese and Part Skim Mozzarella with off odor/taste. Products sold under Fit & Active, LIDL, Market Pantry, and AHOLD brands with specific UPCs and expiration dates. Consumers should check labels for affected items.
SaputoDec 21, 2017 - Lower riskFood
California Popsicle, Inc. recalls Polly Ann Mango Ice Cream Bar 4 BARS-2.5 FL. OZ. (75mL) TOTAL 10 FL. OZ. (300mL) UPC 7 00730 28866 1
California Popsicle, Inc. recalls Polly Ann Mango Ice Cream Bars due to undeclared milk allergen. Consumers should check UPC 7 00730 28866 1 for affected products.
Polly AnnDec 21, 2017 - Stop using nowConsumer product
Wohali Outdoors Recalls Children's Sleepwear Due to Violation of Federal Flammability Standard; Sold Exclusively at Bass Pro Shops
Wohali recalls children's pajama sets sold at Bass Pro Shops for failing flammability standards, risking burn injuries. Consumers must return sets for Bass Pro gift card refunds.
WohaliDec 21, 2017 - Stop using nowConsumer product
Polaris Recalls RZR XP 4 Turbo Recreational Off-Highway Vehicles Due to Fire Hazard (Recall Alert)
Polaris recalls 2018 RZR XP 4 Turbo off-highway vehicles due to risk of fuel leaks causing fire. Owners must stop using and contact a dealer for free repair.
PolarisDec 21, 2017 - Stop using nowConsumer product
Melville Direct Recalls Fiber Optic Christmas Trees Due to Fire Hazard (Recall Alert)
Recall of Bits and Pieces Fiber Optic Christmas Trees with fire risk from overheating AC power adapters. Consumers must stop using and contact for refund.
Bits and PiecesDec 21, 2017 - Stop using nowConsumer product
John Deere Recalls Crossover Gator Utility Vehicles Due to Crash Hazard (Recall Alert)
John Deere recalls XUV825, XUV825 S4, XUV855, and XUV855 S4 Crossover Gator utility vehicles with steering shaft separation risk. Consumers must stop using and contact a dealer for free repair.
John DeereDec 21, 2017 - Use cautionConsumer product
Brompton Bicycle Recalls Bicycles Due To Fall Hazard
Brompton recalls folding bicycles with serial numbers 1403284144 to 1705150001 (made April 2014-May 2017) due to potential bottom bracket breakage causing falls.
BromptonDec 21, 2017 - Stop using nowConsumer product
American Honda Recalls Portable Generators Due to Fire and Burn Hazards
Honda recalls EB2800i and EG2800i portable generators due to carburetor leaks causing fire and burn risks. Stop use immediately.
HondaDec 21, 2017 - Use cautionVehicle
MOBILITY VENTURES MV-1 (2016) recall — Seats
Mobility Ventures is recalling 2011-2016 MV-1 vehicles due to driver seat disengagement risk in rear-end crashes. Owners must get seat track reinforcement kit installed by dealers.
Mobility VenturesDec 20, 2017 - Use cautionVehicle
RAM 1500 (2017) recall — Power Train
Chrysler recalls 2017 RAM 1500s with a potential unintended shift risk. Owners may need software updates and BTSI inspections to prevent rollaways.
ChryslerDec 20, 2017 - Use cautionVehicle
NISSAN VERSA NOTE (2018) recall — Air Bags
Nissan recalls 2018 Versa Note vehicles with side curtain air bags that may detach during deployment, posing injury risks. Owners should contact Nissan for free replacement.
NissanDec 20, 2017 - Use cautionVehicle
LEXUS GX460 (2018) recall — Equipment
Toyota is recalling 2018 Lexus GX460s with incorrect load labels that could cause overloading and crash risk. Owners must get corrected labels free from Toyota.
ToyotaDec 20, 2017 - Use cautionVehicle
AUDI A5 (2018) recall — Air Bags
Volkswagen Group recalls 2018 Audi A5s with head curtain air bags that may not deploy correctly during crashes, increasing injury risk. Owners must contact Audi for free repairs.
AudiDec 20, 2017 - Use cautionVehicle
ALFA ROMEO GIULIA (2018) recall — Service Brakes, Hydraulic
Chrysler is recalling certain 2018 Alfa Romeo Giulia vehicles due to potential contaminated brake fluid that may reduce braking performance, increasing crash risk. Owners will receive free brake system inspections.
Alfa RomeoDec 20, 2017 - Lower riskMedical device
Medtronic Neurosurgery recalls Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, Medtronic Clip Gun Scalp Clip Kit (Qty
Medtronic recalls specific scalp clip kits due to inadequate packaging performance. Affected models and lots may not meet current safety standards. Consumers should check their product details and follow official instructions.
MedtronicDec 20, 2017 - Lower riskMedical device
OraSure Technologies, Inc. recalls Cocaine Metabolite MICRO-PLATE EIA, Catalog Number: 1122SC, UDI: (0100608337000429(17)180228(10)000
OraSure Technologies recalls cocaine metabolite test kits that may cause false positive results with negative controls. Affected units include specific catalog numbers and expiration dates.
OraSureDec 20, 2017 - Use cautionMedical device
Philips Electronics North America Corporation recalls Allura Xper FD and and Xper FD ORT - Philips X-ray Systems Product Usage: The Allura Xper FD10 and Alllura Xper FD10/10
Philips recalls Allura Xper FD10 and FD10/10 X-ray systems from 2003-2017 with risk of monitor falling if set screws loosen. Learn affected models and safety steps.
PhilipsDec 20, 2017 - Use cautionMedical device
Boston Scientific Corporation recalls SpyScope DS Access and Delivery diagnostic biliary catheter, M00546600
Boston Scientific recalls SpyScope DS Access and Delivery diagnostic biliary catheters with a potential risk of bleeding due to a protruding sleeve. Affected units include specific serial numbers.
Boston ScientificDec 20, 2017 - Use cautionMedical device
Integra LifeSciences Corp. recalls The humeral stems trials are packaged in a kit for Titan Modular Shoulder System under the following labeling: Catalog
Integra LifeSciences recalls humeral stem trials for Titan Modular Shoulder System due to reported breakage during insertion or extraction, causing delays in surgery. Affected items include specific catalog numbers and lot numbers.
Integra LifeSciencesDec 20, 2017 - Use cautionMedical device
Merit Medical Systems, Inc. recalls Flex-Neck Classic Peritoneal Dialysis Catheter (Pediatric) Product Usage: If the patient is a suitable candidate for
Merit Medical recalls pediatric peritoneal dialysis catheters due to potential mix-up with adult models. Check lot numbers H1027245 to H99507: if your child uses this catheter, stop using it immediately.
Merit MedicalDec 20, 2017 - Lower riskMedical device
Nidek Inc. recalls AUTO REF/KERATOMETER ARK-1s
Nidek recalls specific ARK-1s models due to possible dioptric value differences between subjective and objective measurement modes. Affected units may have inaccurate eye measurements.
NidekDec 20, 2017 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls Disposable Drill Kit which includes two drill bits, two drill stops, and two adjustment wrenches, sterile. The drill
Ad-Tech Medical recalls disposable drill kits with possible mix-up of 2.4mm and 2.8mm drill bits. These kits are used for cranial surgery and may cause errors if used incorrectly.
Ad-Tech MedicalDec 20, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC NAIL 125 DEG X 11MM STER TROC NAIL 130 DEG X 11MM STER
Zimmer Biomet recalls ACE Trochanteric Nail System models due to failed clinical analysis in device performance reviews, potentially affecting fracture treatment outcomes.
Zimmer BiometDec 20, 2017 - Stop using nowDrug
Fresenius Medical Care Renal Therapies Group, LLC recalls DELFLEX Peritoneal Dialysis Solution, 2.5% Low Mg/Low Ca Single Bag, packaged in a) 3L (4 pack, NDC 49230-209-30), b) 2
Fresenius Medical Care recalls DELFLEX Peritoneal Dialysis Solution due to leakage risk. This affects specific 3L and 2L bags with certain lot numbers. Patients should contact the manufacturer for guidance.
Fresenius Medical CareDec 20, 2017
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