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
34,893 found- Use cautionVehicle
KENWORTH T880 (2017) recall — Exterior Lighting
PACCAR recalls 2017 Kenworth T880 trucks with spotlight circuit short that may cause fire at cab fuse block. Owners must have polyfuse switch replaced with standard fuse free of charge.
PACCARJul 25, 2017 - Lower riskMedical device
Arrow International Inc recalls ARROW PICC powered by ARROW VPS Stylet, Product Codes: CDC-35052-VPS and CDC-35041-VPS. Peripherally Inserted Central
Arrow recalls PICC catheter kits with incorrect catheter sizes that could delay treatment. Affected kits have specific product codes and batch numbers. Contact Arrow for replacement.
ArrowJul 25, 2017 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls Syngo Imaging version V31 (model # 10014063) is a Picture Archiving and Communication System (PACS) intended to
Siemens recalls Syngo Imaging version V31 (model 10014063) due to potential data loss affecting medical imaging diagnoses. Affected units include specific serial numbers listed in the recall notice.
SiemensJul 25, 2017 - Lower riskDrug
Teva Pharmaceuticals USA recalls Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials
Teva Pharmaceuticals USA recalls Albuterol Sulfate Inhalation Solution with high impurities. Products may contain unsafe levels of related compound D. Check lot numbers for affected batches.
Teva Pharmaceuticals USAJul 25, 2017 - Use cautionFood
Gold Medal Products Co recalls CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
Gold Medal Products Co recalls Corn Treats Concentrated Caramel Corn Mix due to missing ingredient statement and undeclared soy. Check your lot numbers.
Gold MedalJul 25, 2017 - Stop using nowConsumer product
Quality Foam Recalls Mattresses Due to Violation of Federal Mattress Flammability Standard
Quality Foam recalls CF model mattresses with white, blue, or green vinyl covers due to failing federal flammability standards. Consumers must stop using and get a free compliant cover.
Quality FoamJul 25, 2017 - Use cautionConsumer product
Polaris Recalls RZR 170 Recreational Off-Highway Vehicles Due to Fuel Leak, Fire Hazards
Polaris recalls 2015-2017 RZR 170 off-highway vehicles due to fuel tank cracks and wiring overheating that could cause leaks or fires. Affected models have specific color and model year markings.
PolarisJul 25, 2017 - Stop using nowConsumer product
Outxpro Mosquito Zapper LED Light Bulbs Recalled by R & D Products Due to Shock Hazard; Sold Exclusively at Amazon.com (Recall Alert)
R&D Products recalls Outxpro 2-in-1 mosquito zapper LED light bulbs due to risk of electrical shock from base separation. Consumers must stop using and contact for free repair.
R&D ProductsJul 25, 2017 - Use cautionMeat & poultry
Stefano's Foods, Inc. Recalls Meat Products Due To Misbranding and Undeclared Allergen
USDA FSIS recalls 981 pounds of Stromboli products from June 2017 due to undeclared egg allergen and misbranding. Consumers urged not to consume and dispose of items.
Stefano's FoodsJul 24, 2017 - Use cautionVehicle
TEMSA TS45 (2016) recall — Engine
Temsa is recalling certain 2014-2018 TS45 motorcoaches due to air bellow cover bending that may contact tires, risking flat tires and crashes. Owners must get free replacement covers.
TemsaJul 24, 2017 - UnratedMedical device
ConforMIS, Inc. recalls Total Knee Replacement , Catalog/Model # TPS-111-1111, UDI: +M572TPS1111111021/$$+31712310398482- and
ConforMIS recalls total knee replacement kits with model TPS-111-1111 that have mislabeled implant kits. Affected units include specific serial numbers and expiration dates. Consumers should contact the manufacturer for details.
ConforMISJul 24, 2017 - Use cautionMedical device
Richard Wolf GmbH recalls Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue
Richard Wolf recalls Artholine Punch B 4 surgical tools due to potential burr injury risk when opening the device. Affected units have product number 89140.0105 and lot number 4500197481.
Richard WolfJul 24, 2017 - Use cautionMedical device
X-Laser Llc recalls X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII,
X-Laser recalls Aurora, Caliente Aurora, PSX-400, Mobile Beat Max models due to potential laser safety hazards when used in auto or music modes. Affected users should check their product details.
X-LaserJul 24, 2017 - Lower riskMedical device
ZIMMER ORTHOPEDIC MFG LTD recalls NexGen LPS Femoral Component, Left and Right, Size G Replaces the femoral condyle of the knee joint in Total Knee
Zimmer recalls NexGen LPS Femoral Component (Size G) due to potential packaging foam breach during shipping. Affected items have specific lot numbers. Consumers should contact Zimmer for details.
ZimmerJul 24, 2017 - Stop using nowMedical device
Smith & Nephew, Inc. recalls smith&nephew POLARSTEM(TM) Femoral Stems with Ti/HA (Standard, Lateral, Valgus and Collar), REF 76102260, NON STERILE,
Smith & Nephew recalls POLARSTEM femoral stems with Ti/HA (Standard, Lateral, Valgus, Collar) due to potential Cardan joint fracture after multiple surgeries. Affected units have specific lot numbers.
Smith & NephewJul 24, 2017 - UnratedMedical device
Sorin Group Italia SRL - CRF recalls Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardioverter defibrillator,
Sorin Group recalls Platinium VR DF4 1240 ICDs with model TDF035U due to potential overconsumption after electrostatic discharge during surgery or MRI scans. Affected patients should contact manufacturer for guidance.
Sorin GroupJul 24, 2017 - Lower riskMedical device
Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc. recalls 3-Way Standardbore Stopcock. Product Code: AMS-100.
Churchill Medical Systems recalls 3-Way Standardbore Stopcocks (AMS-10:1706064D) due to potential gaps in packaging adhesive that could compromise sterility. Affected users should contact the company for details.
Churchill Medical SystemsJul 24, 2017 - Stop using nowMedical device
Epimed International recalls RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet,
Epimed recalls 10-unit sterile epidural needles due to potential partial seal failure, risking infection. Affected items have specific lot numbers and are for medical use only.
Epimed InternationalJul 24, 2017 - Lower riskDrug
Teva Pharmaceuticals USA recalls Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA
Teva Pharmaceuticals recalls 20mg Famotidine tablets due to weight specification failure. This may affect medication accuracy. Contact for details.
Teva PharmaceuticalsJul 24, 2017 - Stop using nowDrug
EZWeightLossTX LLC recalls LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
LaBri's Body Health recalls Atomic 60 Capsules due to being marketed as dietary supplements but containing unapproved drug sibutramine. Consumers should stop using these products immediately.
LaBri's Body HealthJul 24, 2017 - Stop using nowConsumer product
iRover Recalls Self-Balancing Scooters/Hoverboards Due to Fire Hazard
iRover recalls self-balancing scooters and hoverboards with model numbers 87644 and : lithium-ion batteries may overheat, causing fire or explosion. Return for free UL2272-certified replacement.
iRoverJul 24, 2017 - Lower riskMedical device
Qiagen, GmbH recalls QIAamp DSP Virus Kit Cat. No. 60704
Qiagen recalls specific lots of QIAamp DSP Virus Kit (Cat. No. 60704) due to potential decreased performance in analytic workflows. Affected lots include 154025928, 154027751, 154029053, 154029743, and 154029744.
QiagenJul 22, 2017 - Lower riskFood
D & D Foods, Inc. recalls Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Net Wt. 29 oz (1 lb 13 oz) 1.81 lb (822 g), West Des Moines,
Hy-Vee recalls 16" Thin Crust Cheese Pizza with soy lecithin not declared on ingredients list. Consumers should check UPC 288942 611991 for affected products.
Hy-VeeJul 22, 2017 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls FUJINON ED-530XT. This device is intended for the visualization of the duodenum and upper digestive tract, specifically
Fujifilm Medical Systems recalls ED-530XT endoscopy devices due to potential inadequate reprocessing risks. All units are affected; replacement of parts and new manual issued.
Fujif: Medical SystemsJul 21, 2017 - Use cautionMedical device
Howmedica Osteonics Corp. recalls Accolade and Restoration hip product; Catalog Number: 6720-0837 and 6721-0737
Howmedica recalls Accolade and Restoration hip implants with catalog numbers 6720-0837 and 6721-0737 due to potential contamination from unsealed sterile barriers.
HowmedicaJul 21, 2017 - Lower riskMedical device
Helena Laboratories, Corp. recalls SPIFE ImmunoFix-6 Kit, Cat. No. 3401, 3401T, For In-Vitro Diagnostic Use. The firm name on the label is Helena
Helena Laboratories recalls SPIFE ImmunoFix-6 diagnostic kits with missing control wells that could lead to inaccurate test results. Affected kits have specific lot numbers and expiration dates.
HelenaJul 21, 2017 - Use cautionMedical device
Edwards Lifesciences, LLC recalls Certitude Delivery System and any associated Multipacks Models - 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A Product
Edwards Lifesciences recalls Certitude Delivery System models 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A due to potential molding overflow defect that could detach during use and embolize into the patient.
Edwards LifesciencesJul 21, 2017 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls MA3320-PM Premium Adult - SYK Mistral-Air Premium Blankets. MODEL #: MA3302-PM. CATALOG #(s): MA3302-PM
Stryker recalls Mistral-Air Premium Blankets (model MA3302-PM) that may conduct electricity during high-energy defibrillation, risking electrical shock. Affected units include specific lots.
StrykerJul 21, 2017 - Stop using nowMedical device
Synthes (USA) Products LLC recalls 11MM/130 Degree Titanium Trochanteric Fixation Nail 380MM/Right, Sterile
Synthes recalls sterile titanium trochanteric fixation nails with missing locking mechanisms. Affected lot H302839 expires Jan 2026. Stop using immediately to prevent injury.
SynthesJul 21, 2017 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.
Implant Direct recalls Swish Duo-Grip Healing Collar (part 9048-13H) due to incorrect component size in some packages. This may cause improper fit during dental implant procedures.
Implant DirectJul 21, 2017
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83,389 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.