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- Use cautionVehicle
TOYOTA SEQUOIA (2019) recall — Electrical System
Toyota recalls 2019 Sequoia vehicles with faulty airbag ECU that may not deploy in crashes. Owners must update software to prevent injury risk.
ToyotaApr 10, 2018 - Use cautionMedical device
Accuray Incorporated recalls CyberKnife M6, Part Numbers: a) 0660000: CyberKnife Treatment Delivery System b) 053101-010: CyberKnife M6 FI Treatment
Accuray recalls CyberKnife M6 treatment systems with specific part numbers and serials due to risk of unintended collimator housing drop during housing exchange workflows.
AccurayApr 10, 2018 - UnratedMedical device
Bard Brachytherapy, Inc. recalls BARD¿ BrachySource¿ Iodine125 radioactive seeds consist of a welded titanium capsule containing the I125 absorbed onto
Bard recalls Iodine125 radioactive seeds with incorrect dosage levels sent to hospitals. One hospital received 0.28mCi seeds instead of 0.36mCi and vice versa. Affected products include seeds in reusable and shielded applicators.
BardApr 10, 2018 - UnratedDrug
Pharmedium Services, LLC recalls Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL), Rx only, PharMEDium
PharMEDium Services recalls vasopressin injection due to cGMP deviations. This medication is prescription-only and may pose risks if used improperly.
PharMEDiumApr 10, 2018 - UnratedDrug
Aidarex Pharmaceuticals LLC recalls Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00
Aidarex Pharmaceuticals recalls Ferrous Sulfate 325mg tablets with foreign tablets/capsules. Check batch numbers 57909-1 (exp 04/30/2019) and 57909-2 (exp 06/30/2019) for affected units.
Aidarex PharmaceuticalsApr 10, 2018 - Lower riskDrug
Pharmalucence, Inc. recalls Kit for the Preparation of Technetium TC-99M Mebrofenin, 45 mg in 10 mL (5 count), NDC 45567-0455-1 and (30 count), NDC
Pharmalucence recalls kits for Technetium TC-99M Mebrofenin due to failed stability specifications. These kits may degrade over time, posing risks to medical procedures.
PharmalucenceApr 10, 2018 - UnratedFood
Riddhi USA Inc. recalls All dietary supplements manufactured and distributed by Riddhi USA Inc.
Riddhi USA Inc. is recalling all dietary supplements they manufactured and distributed due to a legal requirement under a Consent Decree. No specific product details or safety risks are mentioned in the recall notice.
Riddhi USAApr 10, 2018 - Stop using nowFood
Ohio Hickory Harvest Brand Products Inc. recalls Liberty Snacks Honey Roasted CASHEWS Net Wt. 1.2 oz (#g) DISTRIBUTED BY Liberty Candy & Nuts Inc. 347.945.0540
Liberty Snacks recalls 1.2 oz Honey Roasted Cashews due to positive Listeria monocytogenes test results. Check your lot number and UPC.
Liberty SnacksApr 10, 2018 - Lower riskFood
Columbia Gorge Gluten Free recalls Cinnamon Sugar Cookie, Brand name Columbia Gorge Gluten Free. Packaged in a plastic bag for wholesale purposes. The
Columbia Gorge Gluten Free recalls cinnamon sugar cookies due to incorrect milk labeling. The product claims no dairy but contains milk. No specific action steps provided in recall notice.
Columbia Gorge Gluten FreeApr 10, 2018 - Stop using nowConsumer product
BRP Recalls All-Terrain Vehicles Due to Crash Hazard (Recall Alert)
BRP recalls 2017 Can-Am Outlander and Outlander Max ATVs with dynamic power steering shaft that can break, causing loss of steering control. Consumers must stop using and contact a dealer for free repair.
BRP Can-AmApr 10, 2018 - Lower riskMedical device
Smith & Nephew, Inc. recalls smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING, REF CATALOG NUMBER 71440014 The GENESIS II Knee System
Smith & Nephew recalls Genesis II knee bushings with a laser marking error that could cause incorrect implant placement. Affected units have a specific lot number and require verification.
Smith & NephewApr 9, 2018 - Stop using nowMedical device
Terumo Medical Corp recalls Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
Terumo recalls Angio-Seal Evolution Vascular Closure Device (Cat. No. C610135) due to potential failure in use. Affected units may not function as intended and should not be used.
TerumoApr 9, 2018 - UnratedMedical device
VGI Medical, LLC recalls VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit
VGI Medical recalls lateral interbody fusion instrument kits with unvalidated automated cleaning process. Affected lots and model numbers listed. No remedy provided in official notice.
VGI MedicalApr 9, 2018 - Use cautionMedical device
Cenorin, LLC recalls HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model
Cenorin recalls HLD Systems 600 Series Washer/Pasteurizers with terminal block overheating risk. Affected models include 610HT (115V/230V) with specific serial numbers. Stop using immediately to prevent fire or burn injuries.
CenorinApr 9, 2018 - Use cautionMedical device
Covidien LLC recalls EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -
Covidien recalls hemorrhoid and prolapse stapler sets with DST Series Technology 3.5MM for potential improper staple formation causing bleeding or anastomotic leaks.
CovidienApr 9, 2018 - Lower riskMedical device
BioMerieux SA recalls VIDAS FSH, Ref 30407-01, IVD, Rx. The firm name on the label is bioMerieux SA, France. For use on the instruments of
BioMerie: VIDAS FSH test (Ref 30407-01) recalled due to potential invalid calibration with low calibrator S1. Affected units distributed in the U.S. with lot #1005888210.
BioMerieuxApr 9, 2018 - Lower riskDrug
LEADIANT BIOSCIENCES, INC recalls Cystaran (cysteamine ophthalmic solution) 0.44%, 15 mL bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co. Inc.
Leadiant Biosciences recalls Cystaran 0.44% ophthalmic solution due to subpotent cysteamine hydrochloride. Affected lots expire June 2018 or July 2018. Do not use if you have this product.
Leadiant BiosciencesApr 9, 2018 - Lower riskDrug
Noven Pharmaceuticals, Inc. recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches Rx Only NDC
Noven Pharmaceuticals recalls Daytrana (methylphenidate transdermal system) due to adhesive issues that could lead to incorrect drug delivery. This medication is prescription-only and contains 30 patches delivering 10 mg over 9 hours.
NovenApr 9, 2018 - Stop using nowFood
Whole Foods Market recalls Explorateur French Triple Cr¿me cheese (under the names Explorateur, Explorateur French Triple Cr¿me Cheese and
Whole Foods Market recalls Explorateur French Triple Creme cheese due to potential Listeria monocytogenes contamination. Check lot codes and dates.
Whole Foods MarketApr 9, 2018 - Use cautionMeat & poultry
J.T.M. Provisions Company Recalls Beef Products Due to Possible Foreign Matter Contamination
J.T.M. Provisions recalls 14,525 pounds of pulled barbequed beef products that may contain rubber. Consumers are urged not to consume these items and should discard or return them.
J.T.M. ProvisionsApr 7, 2018 - Lower riskMedical device
Rockwell Medical, Inc recalls DriSate¿ Product Code DR-145 The acid concentrate powders and liquids are indicated for use in acute and chronic
Rockwell Medical recalls DriSate DR-145 product code with sodium bicarbonate contamination in dextrose bags. This may affect hemodialysis treatments. Learn if you have the product and what to do.
Rockwell MedicalApr 7, 2018 - Lower riskFood
Stewart's Shops Corp. recalls Chocolate Peanut Butter Cup Ice Cream, packaged in a 16 oz. cardboard container, UPC 082086444688
Stewart's Shops recalls chocolate peanut butter cup ice cream with a chocolate lid that may cause spills. Products sold with UPC 082086444688 from 8/23/2018 are affected.
Stewart's ShopsApr 7, 2018 - Use cautionVehicle
AUDI A6 (2018) recall — Air Bags
Volkswagen is recalling 2018 Audi A6s with a faulty airbag system that may not deploy in crashes, risking injury. Owners must contact Audi for a free repair kit.
AudiApr 6, 2018 - Lower riskMedical device
MHC Medical Products LLC recalls EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
MHC Medical Products recalls EasyTouch 29G 1ml insulin syringes with incorrect lot numbers on shelf cartons. This may cause confusion in tracking insulin batches.
MHC Medical ProductsApr 6, 2018 - Lower riskMedical device
AROA Biosurgery, LTD. recalls OviTex 1S Reinforced BioScaffold 4x8cm, Part Number F10256-0408G
AROA Biosurgery recalls OviTex 1S Reinforced BioScaffold 4x8cm (Part F10256-0408G) due to potential degradation of suture material after 18 months, which may affect device strength.
AROA BiosurgeryApr 6, 2018 - UnratedMedical device
Orthofix, Inc recalls Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part
Orthofix recalls specific Rival Reduce fracture plating screws due to improper surgical engagement during procedures. Affected items have unique identifiers; contact Orthofix for replacement.
OrthofixApr 6, 2018 - Lower riskDrug
Sandoz Incorporated recalls Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz,
Sandoz recalls 75mg/50mg Triamterene-Hydrochlorothiazide tablets due to cross contamination with unrelated ingredients like Lisinopril and Mannitol. Affected products were sold in 500-count bottles with specific lot numbers.
SandozApr 6, 2018 - Lower riskFood
The J.M. Smucker Company, Inc. recalls HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
J.M. Smucker recalls HUNGRY JACK Original Pancake & Waffle Mix due to salmonella contamination. Consumers should avoid using affected products to prevent foodborne illness.
J.M. SmuckerApr 6, 2018 - Lower riskFood
Bob's Red Mill Natural Foods, Inc. recalls Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. The label is read in
Bob's Red Mill recalls organic amaranth flour (item 6001C224) due to potential Salmonella contamination. Consumers should stop using affected products to avoid foodborne illness.
Bob's Red MillApr 6, 2018 - Stop using nowFood
TRIANGLE PHARMANATURALS LLC recalls Lifted Kratom Green Maeng Da in 45 gram powder, 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form
Triangle Pharmanaturals LLC recalls Lifted Kratom Green Maeng Da products due to potential Salmonella contamination. Check your bottles and stop using them.
Lifted KratomApr 6, 2018
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