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
35,006 found- Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls Computed Tomography X-ray System; Model uCT 530; Rx; UDI: (01) GTIN: 06971576831012 - Product Usage: intended to
Shanghai United Imaging Healthcare recalls uCT 530 CT scanners with uneven metal edges that could cause sharp injuries. Affected units have specific serial numbers and were sold with certain GTINs. Contact for repair or replacement.
Shanghai United Imaging HealthcareJun 20, 2020 - Use cautionVehicle
GRAND DESIGN REFLECTION (2018) recall — Electrical System
Grand Design recalls 2016-2018 Reflection trailers due to unsecured wiring connectors that may allow water entry, causing short circuits and fire risk. Owners should contact customer service for free inspections.
Grand DesignJun 19, 2020 - Stop using nowVehicle
FOREST RIVER FR3 (2021) recall — Electrical System
Forest River recalls 2021 FR3 RVs due to a wiring error that could cause leveling jacks to deploy while driving, risking loss of control and crashes.
Forest RiverJun 19, 2020 - Use cautionVehicle
FOREST RIVER SUNSEEKER (2020) recall — Service Brakes, Air
Forest River recalls 2020 Sunseeker motorhomes with potential brake fluid loss due to fender liner contact with brake hoses. Free brake hose replacement and fender liner modification available.
Forest RiverJun 19, 2020 - Use cautionVehicle
FOREST RIVER SURVEYOR (2020) recall — Equipment
Forest River recalls 2020 Surveyor trailers with specific furnaces that may detach, causing carbon monoxide buildup and poisoning risk. Owners must contact customer service for free repairs.
Forest RiverJun 19, 2020 - Use cautionMedical device
Encore Medical, LP recalls EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.
Encore Medical recalls EMPOWR Partial Knee Peg Drill Guide model 800-06-007 due to potential drilling issues that may delay surgery. All units are affected.
Encore MedicalJun 19, 2020 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Alinity ci series System Control Module (SCM); LN 3R70-01 Alinity ci series software versions, 3.1.1 and below
Abbott recalls Alinity ci series System Control Module software versions 3.1.1 and below due to quality control failures. Affected units may have QC failures that could impact testing accuracy.
AbbottJun 19, 2020 - Lower riskMedical device
Argon Medical Devices, Inc recalls ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage:
Argon Medical Devices recalls ClosureFast Micro Introducer Sheath Set (REF MIS-7F1: 7Fr/Ch 2.3mm x11 cm) due to sterile sheaths with different expiration dates. This affects medical devices used in vein/artery procedures.
Argon Medical DevicesJun 19, 2020 - Use cautionMedical device
Becton Dickinson & Company recalls PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151), 2131915 (UDI
Becton Dickinson recalls PowerLoc MAX Power Injectable Infusion Port Access Kits with specific catalog numbers and lot numbers due to potential tubing cracks causing chemical exposure or infection risks.
Becton DickinsonJun 19, 2020 - Stop using nowFood
Mount Franklin Foods LLC recalls 7-Select Yogurt Pretzels Naturally Flavored Vanilla Crunchy Pretzel Covered in a Vanilla Yogurt NET WT 5 OZ (142 g) UPC
Mount Franklin Foods recalls 7-Select Yogurt Pretzels due to undeclared peanuts. Check your lot numbers and best-by dates immediately.
7-SelectJun 19, 2020 - Lower riskFood
Fresh Express Incorporated recalls Little Salad Bar Garden, 12 oz, UPC 4099100082975, Iceberg lettuce, carrots & red cabbage
Fresh Express recalls Little Salad Bar Garden 12oz salads with iceberg lettuce, carrots and red cabbage due to possible Cyclospora contamination. Consumers should stop using these products if purchased before July 3, 2020.
Fresh ExpressJun 19, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal / Pediatric Oxygenators, Model Number: 701047495 -
Maquet recalls Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD neonatal/pediatric oxygenators due to potential failure to securely hold oxygenators during use. Affected units have lot number 70128207.
MaquetJun 18, 2020 - Lower riskMedical device
Mueller Sports Medicine, Inc recalls Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
Mueller Sports Medicine recalls Hybrid Wraparound Knee Support labeled as 'Not made with Natural Rubber latex' due to natural rubber presence. Affected units sold with UPC 074676642178.
Mueller Sports MedicineJun 18, 2020 - Lower riskMedical device
Synthes, Inc. recalls MatrixNEURO Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial
Synthes recalls MatrixNEURO 5mm screws with incorrect 4mm labeling on one lot (30P6198) that could lead to improper bone fixation during surgery.
SynthesJun 18, 2020 - Lower riskMedical device
Chembio Diagnostics, Inc recalls Chembio DPP¿ Micro Reader for use with the DPP¿ COVID-19 IgM/IgG System- Rapid immunochromatographic test for the
Chembio Diagnostics recalls DPP Micro Reader for COVID-19 antibody testing due to FDA revocation of emergency use authorization. Affected units have model 70-1069-0 and specific lot numbers. Stop using immediately to avoid inaccurate test results.
ChembioJun 18, 2020 - Lower riskMedical device
Philips North America, LLC recalls Phillips Module Charger, Product #: 989803191031 - Product Usage: This Module Charger is used in the Expression MR400
Philips recalls Module Charger (Product # 989803191031) used with Expression MR400 MRI systems due to poor electrical contact causing charging failure. Affected units manufactured before March 2020.
PhilipsJun 18, 2020 - Use cautionMedical device
Anjon Holdings recalls Anjon Bremer Molded Crown. bone fixation fastener for spinal use. REF number 100048 - Product Usage: Smooth or threaded
Anjon recalls specific spinal fixation fasteners (REF 100048) due to high galling risk in threaded components. Affected units include certain lot numbers sold in the US and internationally.
AnjonJun 18, 2020 - Stop using nowDrug
MICHIGAN HERBAL REMEDIES recalls BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Berry Blast, 500mg CBD, 1 FL. OZ (30 ML) bottles, Distributed by:
MICHIGAN HERBAL REMEDIES recalls BC Hemp Co. CBD oil bottles due to elevated lead levels. Consumers should stop using affected products immediately.
MICHIGAN HERBAL REMEDIESJun 18, 2020 - Lower riskFood
Dr. Praeger's Sensible Foods Inc. recalls Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code R20AJ-01A.
Dr. Praeger's recalls 12oz Sweet Potato Bites variety packs with expiration 4/9/2022 (lot R20AJ-01A) due to possible foreign objects. Consumers should check their product and contact the company for details.
Dr. Praeger'sJun 18, 2020 - Lower riskFood
Trident Seafoods Corporation recalls Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution
Trident Seafoods recalls Gordon Choice Imitation Crab Supreme Style (40 oz) due to possible undeclared egg white. Products produced before June 18, 2020, with specific lot codes are affected. Consumers should check packaging for lot codes and expiration dates.
Trident SeafoodsJun 18, 2020 - Lower riskFood
Fresh Express Incorpated recalls Fresh Express Chopped Kit SOUTHWEST TOTAL NET WT. 11.5 oz (326g) plastic bag. FRESH EXPRESS INCORPORATED P.O. BOX
Fresh Express recalls Southwest Chopped Kit bags with undeclared allergens wheat, soy, cashews, and coconut due to incorrect condiment packets during production. Consumers should check product codes and contact the company for details.
Fresh ExpressJun 18, 2020 - Use cautionFood
Coca Cola recalls Coke Zero Sugar 20 oz UPC 049000040869
Coca Cola recalls 20oz Coke Zero Sugar bottles with UPC 049000040869 (SEP0720LWA) due to potential glass fragments. Consumers should check their bottles and contact Coca Cola for details.
Coca ColaJun 18, 2020 - Stop using nowConsumer product
Recreational Off-Highway Vehicles Recalled by American Honda Due to Crash and Injury Hazards (Recall Alert)
Honda recalls 2019-2020 Pioneer 1000 and Talon 1000 side-by-side vehicles that may roll when parked, causing crashes. Owners must stop using and get repairs.
HondaJun 18, 2020 - Use cautionConsumer product
Modus Furniture Recalls Dressers Due to Tip-Over and Entrapment Hazards: In-Home Remedy May be Delayed Due to COVID-19 Restrictions; Keep Product Away from Children (Recall Alert)
Modus Furniture recalls Brighton, Travis, and Bevelle dressers with tapered feet (2017-2019) due to tip-over risks. Keep children away until repair. Free replacement kits and installation offered.
Modus FurnitureJun 18, 2020 - Use cautionConsumer product
Lochinvar Recalls Condensing Residential Boilers Due to Risk of Carbon Monoxide Poisoning
Lochinvar recalls residential condensing boilers sold after August 2016 due to risk of carbon monoxide poisoning from deteriorating flue grommets. Consumers must schedule free repairs with a technician.
LochinvarJun 18, 2020 - Lower riskMeat & poultry
La Bodega Meat LLC Recalls Beef Products Distributed Without Benefit of Import Re-Inspection
USDA FSIS recalls 83,038 pounds of raw beef products imported without re-inspection. Consumers urged not to consume these items, which may pose food safety risks.
La Bodega MeatJun 17, 2020 - Use cautionVehicle
VOLKSWAGEN JETTA (2020) recall — Service Brakes, Hydraulic
Volkswagen recalls one 2020 Jetta with potential brake caliper bolt loosening, risking crash. Owners must contact customer service for free front brake caliper bolt replacement.
VolkswagenJun 17, 2020 - Lower riskMedical device
Resource Optimization & Innovation LLC recalls regard Migrating Indicator, STEAM Migrating Indicator Strips, REORDER # 335576REG - Product Usage: The integrating
Regard Migrating Indicator Strips may malfunction during steam sterilization cycles, failing to enter the 'accept' window. Affected units from Lot 719 should be checked for proper function.
RegardJun 17, 2020 - Lower riskMedical device
FHC, Inc. recalls FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Usage: intended to record and stimulate electrophysiological
FHC recalls GL5 Main Processing Units with serial numbers 45695, 48871, 48873, 48874, 46195, 46198 due to potential ESD interference. Affected units may malfunction during high-voltage events.
FHCJun 17, 2020 - UnratedMedical device
Wellspect HealthCare (Division of DENTSPLY IH AB) recalls LoFric Origo, Tiemann, 16in, FR12 urinary catheters
Wellspect HealthCare recalls certain LoFric Origo urinary catheters with a potential defect in the distal tip. Affected units include Lot #450422. Consumers should contact Wellspect for details.
Wellspect HealthCareJun 17, 2020
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83,594 recalls tracked · 72,041 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.