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. 2,598 recalls have been distributed to Idaho in the last 12 months.
Showing 3761–3780 of 48,215 recalls
Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin Chewable tablet 81 mg Recalled by Safecor Health, LLC Due to cGMP...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Carbonate Chewable 500 mg Recalled by Safecor Health, LLC Due to...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docusate Sodium 250 mg Recalled by Safecor Health, LLC Due to cGMP...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin B1 Recalled by Safecor Health, LLC Due to cGMP Deviations:...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin D3 Recalled by Safecor Health, LLC Due to cGMP Deviations:...
The Issue: cGMP Deviations: Observations were made that some blister card-foils were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1....
The Issue: Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriALTIS TORQUE LIMITER Recalled by Gauthier Biomedical, Inc. Due to An out...
The Issue: An out of specification component may result in the device exhibiting torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) KIT Recalled by Cardinal Health 200, LLC...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) UROLOGY ROBOTIC PACK Recalled by Cardinal...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Presource Kits: 1) LARYNGOSCOPY PACK Recalled by Cardinal...
The Issue: Potential for endotoxin contamination in non-sterile surgical strips and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.