Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,660 recalls have been distributed to Alabama in the last 12 months.
Showing 4901–4920 of 28,641 recalls
Recalled Item: Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...
The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...
The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.