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
34,960 found- Use cautionMedical device
Haag-Streit USA Inc recalls HS Hi-R NEO 900A NIR Reference # 657 822 Serial # from 101 Product Usage: A wide range of surgical interventions are
Haag-Streit recalls specific models of surgical microscopes with software errors that may cause incorrect surgical measurements during procedures. Affected units include certain FS 2-21, FS 2-25, and FS 3-45 floor stands with specific serial numbers and software versions.
Haag-StreitJul 31, 2019 - Use cautionMedical device
Becton Dickinson & Company recalls BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This
Becton Dickinson recalls BD Vacutainer Push Button Blood Collection Sets with catalog number 368356 due to risk of front and rear barrel separation during use, potentially causing injury.
Becton DickinsonJul 31, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Top; Models #11061640 Product Usage: This computed tomography system is intended to generate and process
Siemens recalls SOMATOM go.Top CT scanners with model #11061640 due to risk of injector holder falling off, potentially causing injury during medical procedures.
SiemensJul 31, 2019 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 07613327277319 Product Usage: The C2 Nerve Monitor System is intended
Stryker recalls C2 Nerve Monitor models due to possible use errors causing nerve injury during surgery. Affected units include specific serial numbers and models sold for intra-operative nerve monitoring.
StrykerJul 31, 2019 - Stop using nowConsumer product
London Bridge Recalls Sock and Wrist Rattle Sets Due to Choking Hazard
London Bridge recalls infant sock and wrist rattle sets (0-6 months) due to small rattles that can detach and cause choking. Consumers should stop using and return items for a refund.
London BridgeJul 31, 2019 - Stop using nowConsumer product
Dorel Juvenile Group USA Recalls Inclined Sleepers Due to Safety Concerns About Inclined Sleep Products
Dorel recalls two infant inclined sleepers due to risk of infants rolling over and causing fatalities. Affected models include Eddie Bauer Slumber and Soothe Bassinet (BT055CSY) and Disney Baby Doze and Dream Bassinet (BT071DHS).
DorelJul 31, 2019 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material
Siemens recalls Artis zee and Artis Q/Q.zen interventional fluoroscopy systems with patient tables that may have cracks causing table parts to detach and fall, risking injury to patients and staff.
SiemensJul 30, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000 Product Usage: automated, clinical chemistry
Siemens recalls Atellica CH 930 analyzers with software versions 1.19.2 or older that may give incorrect hemolysis and lipemia test results.
Siemens HealthcareJul 30, 2019 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls Digital Medical X-ray Imaging System, Model: uDR 596i, uDR 592h
Shanghai United Imaging Healthcare recalls uDR 596i and uDR 592h X-ray systems due to reversed spine positioning labels, risking repeat patient exposures. Affected units have specific serial numbers and were sold with certain DI/GTIN codes.
Shanghai United Imaging HealthcareJul 30, 2019 - Lower riskMedical device
Eizo Corporation recalls RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in
Eizo recalls specific RadiForce GX560 monochrome LCD monitors for occasional marble patterns, which may affect medical imaging accuracy. Affected models include 0FTD2347 and 0FTD2379.
EizoJul 30, 2019 - Use cautionMedical device
Teleflex Medical recalls Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF
Teleflex Medical recalls specific sizes of Sheridan EZ-ENDO connectors due to reported disconnections from breathing tubes, potentially causing insufficient oxygenation and requiring medical intervention.
Teleflex MedicalJul 30, 2019 - Lower riskFood
Ruleau Bros, Inc. recalls Door County Whitefish Smoked Whitefish Pate 8oz plastic tub UPC 8 55356 00402 4 Keep Refrigerated 12 retail units per
Ruleau Bros recalls 12 units of Door County Smoked Whitefish Pate due to undeclared anchovy, egg, and soy ingredients. Keep refrigerated and check lot numbers for affected products.
Ruleau BrosJul 30, 2019 - Lower riskFood
Green Water, LLC recalls Taspen s Organics,Happy Momma Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce
Green Water, LLC recalls certain lots of herbal tinctures due to potential Salmonella contamination. Consumers should avoid using affected products to prevent foodborne illness.
Taspen s OrganicsJul 30, 2019 - Stop using nowConsumer product
Tristar Products Recalls Magnetic Trivets Due to Magnet Ingestion Hazard (Recall Alert)
Tristar Products recalls magnetic trivets sold with Copper Chef cookware due to risk of magnets detaching and causing serious intestinal injuries if swallowed by children.
Tristar ProductsJul 30, 2019 - Use cautionVehicle
MAZDA MAZDA3 (2019) recall — Visibility
Mazda recalls 2019 Mazda3 vehicles with manual dimming mirrors due to risk of rearview mirror detachment causing reduced visibility and crash risk. Owners must contact Mazda for free replacement.
MazdaJul 29, 2019 - Lower riskMedical device
MOTEK MEDICAL B.V. recalls Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to
MOTEK Medical recalls Body Weight Support Light model RB011 due to rare risk of yoke detaching from cable guide during gait training. Affected users should check model numbers listed in the recall notice.
MOTEK MEDICALJul 29, 2019 - Lower riskMedical device
The Binding Site Group, Ltd. recalls OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565
The Binding Site Group recalls OPTILITE IgM Kit (REF: NK012.OPT.A) due to potential calibration errors that could lead to false patient results and delayed testing.
The Binding Site GroupJul 29, 2019 - Lower riskMedical device
ICU Medical Inc recalls Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary
ICU Medical recalls Plum Microbore Infusion Sets with Inline Filters labeled as Primary due to potential fluid leakage from air vents. Affected units have specific product codes and lot numbers. Consumers should check their units and contact the company for details.
ICU MedicalJul 29, 2019 - Lower riskDrug
Upsher Smith Laboratories, Inc. recalls Bexarotene Capsules, 75 mg, 100 capsules per bottle, Rx Only, Manufactured for: Upsher-Smith Laboratories, LLC, Maple
Upsher Smith recalls 75mg Bexarotene Capsules due to failed dissolution specifications. Rx-only capsules may not release medication properly. Contact for return instructions.
Upsher SmithJul 29, 2019 - Lower riskDrug
Aurobindo Pharma USA Inc. recalls Simvastatin Tablets, USP 40 mg. Rx Only 1000 Count Bottles Manufactured by: Aurolife Pharma LLC Dayton NJ 08810
Aurobindo Pharma USA recalls 1000-count Simvastatin 40mg tablets due to incorrect lot and expiration dates on some bottles. Affected lots include 05318054B (exp 3/2021).
Aurobindo PharmaJul 29, 2019 - Lower riskFood
Kerry, Inc recalls Breader, Item Number 30753150.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
Kerry recalls 50 lb Breader product with foreign nylon string. Consumers should check item numbers and contact Kerry for details.
KerryJul 29, 2019 - Use cautionMeat & poultry
Premium Foods USA, Inc., Recalls Siluriformes Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 121,151 pounds of Siluriformes fish products imported from Bangladesh and Myanmar without proper import inspection. Consumers urged not to consume or discard items.
Premium FoodsJul 27, 2019 - Lower riskFood
Harvest Sensations, LLC recalls Fresh basil packaged in plastic bags, each weighing one pound. (No label)
Harvest Sensations recalls fresh basil (1lb plastic bags, no label) due to Salmonella contamination. Consumers should avoid eating affected products to prevent foodborne illness.
Harvest SensationsJul 27, 2019 - Stop using nowMeat & poultry
Kent Quality Foods, Inc. Recalls Ready-To-Eat Sausage Products due to Possible Foreign Matter Contamination
Kent Quality Foods recalls ready-to-eat polish sausage products that may contain pieces of flexible pink rubber. Consumers are urged not to consume these products and should discard or return them to the store.
Kent Quality FoodsJul 26, 2019 - Use cautionVehicle
TEMSA TS45 (2016) recall — Steering
Temsa is recalling certain 2014-2019 TS45 buses due to potential hydraulic steering hose leaks that could affect steering and increase crash risk. Owners should contact Temsa for free repairs.
TemsaJul 26, 2019 - Use cautionVehicle
MOTO GUZZI ELDORADO (2016) recall — Service Brakes, Hydraulic
Recall for 2016 Moto Guzzi Eldorado motorcycles with front brake master cylinder issue causing unexpected slowing without warning. Owners must have brakes inspected by dealers.
Moto GuzziJul 26, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Electrical System
Chrysler recalls certain 2019 Ram 1500 vehicles with faulty instrument clusters that may not illuminate warnings, risking crashes. Owners can get free replacements.
ChryslerJul 26, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Giraffe OmniBed Carestation CS1 - Product Usage: The device can be operated as an incubator or as a warmer and can
GE Healthcare recalls Giraffe OmniBed Carestation CS1 models with fasteners that may become detached, risking falls. Check serial numbers for affected units.
GE HealthcareJul 26, 2019 - UnratedMedical device
Becton Dickinson & Co. recalls BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing Catalog Number : 447213
Becton Dickinson recalls BD Kiestra InoqulA+ software version 20.3 for potential specimen-plate mismatch. Affected units have specific catalog and serial numbers. No remedy is stated in the recall notice.
Becton DickinsonJul 26, 2019 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci X Surgical System Surgical System, IS4200, 00886874114216 Product Usage: used with an endoscope, surgical
Intuitive Surgical recalls da Vinci X surgical systems with defective capacitors that could cause vision loss or system errors. Affected units have specific serial numbers; contact for remedy.
Intuitive SurgicalJul 26, 2019
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