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
34,959 found- Stop using nowConsumer product
Amerex Group Recalls Infant Fur Jackets Due to Choking Hazard
Amerex Group recalls infant faux fur jackets because snaps can detach, posing a choking hazard. Contact for a full refund.
Amerex GroupApr 2, 2019 - Use cautionVehicle
VANTAGE AMS EDGE II (2015) recall — Fuel System, Gasoline
Vantage is recalling 2014-2017 AMS Edge II vehicles with potential fuel leaks that could cause fire if near ignition sources. Owners must have fuel tank replaced free of charge by Vantage.
VantageApr 1, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Mobi-C 14mm Distraction Screw, Quick Start. Intended for cervical intervertebral disc replacement. Item Number:
Zimmer Biomet recalls Mobi-C 14mm Distraction Screws with a mislabeled 12mm part on packaging. This could lead to using the wrong size screw during cervical spine surgery. Affected units have item number 0024-LDR.
Zimmer BiometApr 1, 2019 - Use cautionMedical device
Olympus Corporation of the Americas recalls Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be
Olympus recalls MAJ-209 Single Use Suction Valves (model numbers 88H-91H) due to risk of coming apart or getting stuck inside endoscopes during use.
OlympusApr 1, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci SP surgical system
Intuitive Surgical recalls da Vinci SP surgical systems with specific serial numbers due to rare vibration risk when using Adjust Mode near vertical position limit and sustained force on hand controls.
Intuitive SurgicalApr 1, 2019 - Lower riskMedical device
Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
Teleflex Medical recalls RUSCH LASERTUBE (Rubber) units with laser guard foil that may partially separate at edges. Affected units include specific lot numbers and sizes. No remedy is stated in the recall notice.
Teleflex MedicalApr 1, 2019 - Lower riskMedical device
Dornier Medtech America, Inc. recalls Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K1001291 600 micron
Dornier recalls specific laser fiber models used with Medilas D Family Lasers due to pin hole package failures that could compromise product sterility. Affected items include K1001291, K2011824, and other 600 micron fibers. Consumers should check their product details.
DornierApr 1, 2019 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Telmisartan and Amlodipine Tablets 80 mg/5 mg, 30 tablet bottle, Rx only, Manufactured for: Lupin Pharmaceuticals,
Lupin Pharmaceuticals recalls 80mg/5mg Telmisartan and Amlodipine tablets due to impurities that could cause serious injury. Rx-only bottles with specific NDC numbers and expiration dates are affected.
Lupin PharmaceuticalsApr 1, 2019 - UnratedDrug
NingBo Huize Commodity Co.,Ltd. recalls DIPPIN' DOTS SCENTED COTTON CANDY ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by:
DIPPIN' DOTS SCENTED COTTON CANDY ANTIBACTERIAL HAND GEL with 62% ethyl alcohol was recalled due to missing stability testing. This could affect product safety.
DIPPIN' DOTSApr 1, 2019 - Lower riskMedical device
Integra Limited recalls Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra Flowable Wound Matrix is indicated for the
Integra recalls Flowable Wound Matrix (FWD301) due to stability problems during mixing and storage. Affected lots may not maintain proper appearance or strength over time.
IntegraMar 31, 2019 - Lower riskMedical device
Verathon, Inc. recalls GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Verathon recalls GlideScope Video Laryngoscope manual with incorrect low-level disinfection instructions for titanium blades. Affected units include specific revisions and serial numbers. Contact for correction.
VerathonMar 31, 2019 - Lower riskFood
Wholesome Treats, Inc. recalls Breads from Anna Dairy & Corn Free Bread Mix 19oz, carton
Wholesome Treats recalls 19oz corn-free bread mixes due to undeclared flaxseed in product labels. Consumers should check labels for lot number 031921 010201.
Wholesome TreatsMar 31, 2019 - Use cautionMeat & poultry
Market of Choice, Inc. Recalls Pork and Poultry Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 145 pounds of Market of Choice pork and poultry products due to undeclared milk and soy allergens not listed on labels. Consumers urged not to consume these items.
Market of ChoiceMar 30, 2019 - Use cautionMedical device
Thoratec Corp. recalls Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief, Sterile, REF 105581US/105581, RX only, Part of Left
Thoratec recalls Heartmate 3 Sealed Outflow Graft with Bend Relief for potential leaking during implantation. If the C-Ring isn't seated properly, the device may not function during surgery.
ThoratecMar 30, 2019 - Stop using nowFood
LITTLE RED ROOSTER COMPANY recalls NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint packaged in a carton
LITTLE RED ROOSTER COMPANY recalls NadaMoo! Strawberry Cheesecake Non-Dairy Frozen Dessert due to undeclared almonds. Check your carton.
NadaMoo!Mar 30, 2019 - Use cautionVehicle
NEWMAR BAY STAR (2019) recall — Equipment
Newmar is recalling 2018-2019 Bay Star motorhomes due to overheated WiFiRanger power supply risking fire. Owners must have power supply replaced free by dealers.
NewmarMar 29, 2019 - Use cautionVehicle
FOREST RIVER ROCKPORT (2019) recall — Electrical System
Forest River recalls 2017-2019 Rockport work trucks with missing inline fuses that could cause wiring to melt and start a fire. Owners must contact customer service for free fuse installation.
Forest RiverMar 29, 2019 - Use cautionMedical device
Conformis, Inc. recalls Conformis iTotal Hip Replacement System: HBS-033-00xx-010101, (HIP-PATIENT SPECIFIC STEM LEFT)
Conformis recalls specific hip replacement stems due to 3mm discrepancy between iViews measurements and actual implant neck/head lengths, potentially causing improper fit.
ConformisMar 29, 2019 - Lower riskMedical device
Centurion Medical Products Corporation recalls Sterile Nail Clipper Concave Edge (67710)
Centurion Medical recalls sterile nail clippers with compromised pouch seals to prevent contamination. Affected models: Concave Edge (67710), Lot 2018120701, exp 2023-11-30.
Centurion MedicalMar 29, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Prestilix 1600X Prestilix system is a fully integrated remote controlled digital radiology system. It is designed for
GE Healthcare recalls Prestilix 1600X digital radiology systems after reports of Distar CRT monitors falling from wall mounts due to product aging.
GE HealthcareMar 29, 2019 - Lower riskMedical device
PROVIDENCE MEDICAL TECHNOLOGIES recalls Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint
Providence Medical Technologies recalls Ally Bone Screws (PD 32 601 and PD 32 602 models) due to potential dimensional manufacturing errors that could pose safety risks during bone reconstruction procedures.
Providence Medical TechnologiesMar 29, 2019 - Lower riskDrug
X-Gen Pharmaceuticals Inc. recalls Clonidine HCL Injection, 1000 mcg/10mL (100 mcg/mL), 10 ML Single Dose Vial, Rx only, Manufactured for: X-Gen
X-Gen Pharmaceuticals recalls Clonidine HCL injection vials with incorrect concentration labeling. The label shows 500mcg per mL instead of the correct 100mcg per mL, which could lead to improper dosing.
X-GenMar 29, 2019 - UnratedDrug
Jubilant Cadista Pharmaceuticals, Inc. recalls Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx Only, Manufactured by: Jubilant Generics
Jubilant Cadista recalls 12,960 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on tablet edges.
Jubilant CadistaMar 29, 2019 - UnratedFood
Cays LLC recalls Addback Tablet Dietary Supplement 60 tablets per 190cc Oblong WHDPE bottle Net Wet: 85gm (60 tablet wt) UPC-
Cays LLC recalls Addback Tablets due to undeclared ingredients including HPMC, Triacetin, and food dyes. Consumers should check product labels and contact the company for details.
Cays LLCMar 29, 2019 - Use cautionVehicle
RAM 5500 (2018) recall — Exterior Lighting
Blanchat is recalling 2018 RAM 5500 vehicles with Whelen brake lights that may illuminate without pressing the brake pedal, risking crashes. Owners can get free replacement lights.
BlanchatMar 28, 2019 - Use cautionVehicle
FORD F-550 (2018) recall — Exterior Lighting
Blanchat is recalling 2018 Ford F-550 trucks with Whelen brake lights that may illuminate without pressing the brake pedal, risking crashes. Owners can get free brake light repairs.
BlanchatMar 28, 2019 - Use cautionVehicle
FORD F-550 (2018) recall — Exterior Lighting
FES recalls specific 2018 Ford F-550 emergency vehicles due to brake lights illuminating without pedal input. Free replacement available.
FESMar 28, 2019 - Use cautionVehicle
FORD TRANSIT (2018) recall — Seats
Royale recalls 2015-2018 Ford Transit mini-coaches with Freedman GO-ES foldaway seats that may not stay locked during crashes, increasing injury risk. Owners must contact Royale for repair.
RoyaleMar 28, 2019 - Use cautionVehicle
FORD TRANSIT (2018) recall — Seats
Recall of 2018 Ford Transit shuttle vans with Freedman GO-ES Foldaway Seats due to risk of seat cushion not staying locked during crashes.
WaldochMar 28, 2019 - Use cautionVehicle
JEEP CHEROKEE (2019) recall — Seats
Chrysler recalls 2019 Jeep Cherokee vehicles with loose front passenger seat mounting bolts that could increase injury risk during crashes.
ChryslerMar 28, 2019
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