Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 967 recalls have been distributed to Idaho in the last 12 months.
Showing 31121–31140 of 48,215 recalls
Recalled Item: Nabisco Oreo Fudge Creme Original Variety Recalled by Mondelez International...
The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Skinny Bee Diet capsules Recalled by Love My Tru Body Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: presence of undeclared sibutramine,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol...
The Issue: Failed Stability Specifications: Low Out of Specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: manufactured under practices which may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed Dissolution Specifications: The firm was notified that there was a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...
The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...
The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...
The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...
The Issue: Trumpf has identified six incidents of pinched cables.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...
The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.