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. 2,581 recalls have been distributed to Idaho in the last 12 months.
Showing 6821–6840 of 48,215 recalls
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...
The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6...
The Issue: Product has the potential to be contaminated with Cronobacter sakazakii.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Methoxsalen Capsules Recalled by Strides Pharma Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ibuprofen and Famotidine Tablets 800mg/26.6mg Recalled by Ascend...
The Issue: Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Rising Pharma...
The Issue: Presence of Foreign Tablets/Capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MB215R - MILLS DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc Due...
The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MB362R - JACOBSON DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc...
The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Due to An incorrect electrical...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.