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. 1,047 recalls have been distributed to Idaho in the last 12 months.
Showing 14301–14320 of 48,215 recalls
Recalled Item: Affected components are limited to the Monoprice charging cable (Product...
The Issue: Warning Added: Using damaged cables or chargers, or charging when moisture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant 3.5x10 Recalled by Jjgc Industria E Comercio De...
The Issue: 3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle Recalled by Cook Inc. Due to Transseptal needles may...
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261....
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Crescent Knife Recalled by Beaver Visitec International, Inc....
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parent's Choice Rice Baby Cereal. Stage 1 Recalled by Maple Island Inc . Due...
The Issue: Product contains elevated level of inorganic arsenic.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Imipramine Pamoate Capsules 125 mg Recalled by Lupin Pharmaceuticals Inc....
The Issue: Out of specification result observed in a dissolution test at the 9-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ComposiTCP 30 Interference screw D 7- L:25 mm Recalled by SCIENCE & BIO...
The Issue: Mislabeled product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Electrodes Recalled by 3M Company - Health Care Business Due to...
The Issue: Potential for breakage of the ECG electrode carbon stud from the eyelet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis/ Sensis Vibe systems with software VD1X as follows: (1)Sensis...
The Issue: System operator manual states that the system should be rebooted once, every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: CGMP Deviations: Customer complaint for the presence of a staple co-mingled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.