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
34,896 found- Stop using nowVehicle
LOTUS EVORA (2018) recall — Steering
Lotus recalls certain 2018 Evora vehicles due to a steering column assembly error that may not collapse properly in a crash, increasing injury risk.
LotusJun 11, 2018 - Use cautionVehicle
FORD TRANSIT (2018) recall — Seats
National Van recalls 2015-2018 Ford Transits with Freedman GO-ES Foldaway Seats. In crashes, seat backs may move, increasing injury risk. Free repair available.
National VanJun 11, 2018 - Use cautionVehicle
KEYSTONE MONTANA (2019) recall — Service Brakes, Hydraulic
Keystone is recalling 2019 Montana trailers with Legacy package due to potential brake failure. Owners must have brake disc mounting fasteners replaced free by dealers.
KeystoneJun 11, 2018 - Use cautionVehicle
BLUE BIRD BBCV (2019) recall — Electrical System
Blue Bird is recalling 2017-2019 BBCV transit buses with improper alternator cable routing that could cause electrical shorts and fires. Owners must have their wiring checked by dealers by Dec 6, 2018.
Blue BirdJun 11, 2018 - Use cautionMedical device
NxStage Medical, Inc. recalls NxStage Express Fluid Warmer (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A) Product Usage: The NxStage Express Fluid
NxStage recalls Express Fluid Warmers (FW-300 series) due to potential electrical fire if fluid leaks into power receptacle. No injuries reported but 7 smoke/sparks incidents since 2016.
NxStageJun 11, 2018 - Use cautionMedical device
Withings Sas recalls Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-invasive
Withings recalls Nokia BPM+ wireless blood pressure monitors due to potential systolic pressure measurement errors. Check your device details.
NokiaJun 11, 2018 - Lower riskMedical device
ESAOTE S.P.A. recalls MyLab Gamma, Model 7410
ESAOTE recalls MyLab Gamma 7410 ultrasound probes due to overheating risk during prolonged use. No injuries reported but discomfort and skin irritation possible.
ESAOTEJun 11, 2018 - Lower riskMedical device
Philips Healthcare recalls Centron Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic,
Philips Healthcare recalls Centron imaging products for potential shutter reset during procedure changes, affecting vascular and cardiac imaging. Users should check model numbers and contact Philips for guidance.
Philips HealthcareJun 11, 2018 - Lower riskMedical device
Canadian Hospital Specialties recalls MED-RX, Ref 54-1650R 5Fr X 16 inch (40cm) Polyurethane Feeding Tube For Pediatric Use with Orange Radiopaque Stripe and
Canadian Hospital Specialties recalls MED-RX pediatric feeding tubes due to potential incorrect length packaging. Affected units may cause feeding issues if used improperly.
Canadian Hospital SpecialtiesJun 11, 2018 - Lower riskMedical device
Edwards Lifesciences, LLC recalls Edwards SAPIEN 3 Transcatheter Heart Valve (THV), Model: 9600TFX, Size: 26 mm
Edwards recalls SAPIEN 3 Transcatheter Heart Valve (Model 960: 26mm) due to incorrect valve size packaging. Affected units have specific serial numbers and use-by dates.
EdwardsJun 11, 2018 - Use cautionMedical device
Cardinal Health 200, LLC recalls Hydroline Trumpet Valve, Trumpet Valve, 5mm x 28cm Probe, Double Spike, Ref ASU1211, packaged 1/box, 12 boxes/case,
Cardinal Health recalls Hydroline Trumpet Valves due to risk of continuous suction. This may cause injury during medical procedures. Affected items have specific model and lot numbers.
Cardinal HealthJun 11, 2018 - UnratedDrug
BioDiagnostic International recalls Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single application vials and 12 applicators, 8 mL per box,
BioDiagnostic International recalls Monsel's Solution (20% Ferric Subsulfate) due to CGMP deviations. Products packaged as 12 vials and 12 applicators, 8mL per box, manufactured for MedGyn Products. No remedy specified in recall notice.
BioDiagnostic InternationalJun 11, 2018 - Lower riskFood
Absonutrix recalls Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as
Absonutrix recalls Lyfetrition Vitamin B12 bottles that do not contain the listed vitamin B12. Consumers should check product labels for missing vitamin B12.
AbsonutrixJun 11, 2018 - Lower riskFood
The TJX Companies, Inc. recalls FUNKTIONAL FOODS brand SPIRULINA POWDER, NET WEIGHT 3.5 oz (100 g) with UPC Code: 060427570192
The TJX Companies recall FUNKTIONAL FOODS Spirulina Powder (3.5 oz) due to undeclared sulfites at 40 ppm. Consumers should check UPC 060427570192 and lot code F-704101 for affected products.
FUNKTIONAL FOODSJun 11, 2018 - Use cautionVehicle
INFINITI QX50 (2019) recall — Air Bags
Nissan recalls 2019 INFINITI QX50 vehicles where passenger-side knee air bag cover may detach during deployment, increasing injury risk. Owners can get free replacement.
INFINITIJun 9, 2018 - Stop using nowMeat & poultry
Tyson Foods Inc. Recalls Breaded Chicken Products Due to Possible Foreign Matter Contamination
Tyson Foods is recalling approximately 3,120 pounds of frozen breaded chicken tenderloins that may contain blue and clear soft plastic. Consumers should throw away affected products to avoid potential foreign material contamination.
Tyson FoodsJun 8, 2018 - Lower riskMeat & poultry
Venda Ravioli, Inc. Recalls Meat Ravioli Products Produced Without Benefit of Inspection
USDA FSIS recalls 672 pounds of frozen meat ravioli made without federal inspection. Consumers should not eat or throw away recalled products.
Venda RavioliJun 8, 2018 - Use cautionVehicle
NEWMAR DUTCH STAR (2019) recall — Equipment
Newmar is recalling 2018-2019 Dutch Star motorhomes due to entry doors that may open during transit, increasing crash risk. Owners must contact customer service for free door latch adjustment.
NewmarJun 8, 2018 - Lower riskMedical device
Randox Laboratories Ltd. recalls Liquid Cardiac Control - Level 3, cat. no. CQ5053 Product Usage: This product is intended for in vitro diagnostic use,
Randox recalls Liquid Cardiac Control Level : Unacceptable variation in Troponin T assay results may delay critical cardiac marker testing. Affected lots include 4245CK.
RandoxJun 8, 2018 - Lower riskMedical device
Zimmer Surgical Inc recalls Zimmer Dermatone AN, Model No. 88710100
Zimmer recalls Dermatone AN surgical devices with model 88710100 that may have loose control bars or width plates, risking uneven graft thickness during skin graft procedures.
ZimmerJun 8, 2018 - Lower riskMedical device
Bio-Rad Laboratories, Inc recalls MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with
Bio-Rad recalls MRSASelect agar plates (lot numbers 64179161-64192125) due to abnormal coloration and non-characteristic MRSA colonies. Consumers should check their lot numbers and contact Bio-Rad for details.
Bio-RadJun 8, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.
Zimmer Biomet recalls ARCOS Modular Revision Hip System item 11-300: Potential for extended surgery time if components are mixed.
Zimmer BiometJun 8, 2018 - Lower riskMedical device
Ethicon, Inc. recalls PDS Plus Antibacterial Suture-PDS PLUS Undyed Suture 45cm (18") 5-0 Single Armed P-3 Prime Needle Product Code: PDP493G
Ethicon recalls PDS Plus Antibacterial Suture (PDP493G) due to insufficient tensile strength. Affected units may fail during use, risking complications. Contact Ethicon for details.
EthiconJun 8, 2018 - Lower riskMedical device
Stryker Neurovascular recalls Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -
Stryker recalls Synchro2 guidewires with incorrect outer diameter label (0.036mm instead of 0.36mm). This could lead to improper use during medical procedures. Affected units include specific lot numbers and product codes.
StrykerJun 8, 2018 - Lower riskDrug
Qualgen, LLC recalls TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK
Qualgen recalls testosterone pellets with missing lot or expiration dates. Patients should check labels for correct dates to ensure safe use.
QualgenJun 8, 2018 - Lower riskDrug
Ingenus Pharmaceuticals Llc recalls Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, Manufactured for:
Ingenus Pharmaceuticals recalls specific lot numbers of Irinotecan Hydrochloride Injection due to high potency assay results. This may affect cancer treatment safety.
Ingenus PharmaceuticalsJun 8, 2018 - Stop using nowFood
Golden Star Wholesale Inc recalls Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case
Golden Star Wholesale recalls Al Reef dried apricot sour due to undeclared sulfites. Check your product code and distribution dates.
Al ReefJun 8, 2018 - Lower riskFood
T R Toppers, Inc. recalls TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075 GTIN 0 06 51844 10599 6, 7.5 Lbs. (3 x 2.5 Lbs.
TR Toppers recalls chopped chocolate pretzel pieces due to potential peanut contamination. Affected items have specific lot numbers and packaging details. Consumers should check their purchases and contact the company for guidance.
TR ToppersJun 8, 2018 - Lower riskFood
Caito Foods Service, Inc. recalls Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Kroger MIXED SPEARS
Caito Foods recalls mixed melons sold at Kroger stores due to potential Salmonella contamination. Consumers should check UPC 826766139606 for affected products.
Caito FoodsJun 8, 2018 - Use cautionConsumer product
Amerisun Recalls to Repair Snow Blowers Due to Injury Hazard
Amerisun recalls 2015-2017 PowerSmart gas snow blowers with loose pulley bolts that can cause injury. Check for loose bolts and contact for free repair.
AmerisunJun 8, 2018
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