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. 2,566 recalls have been distributed to Alabama in the last 12 months.
Showing 16341–16360 of 28,641 recalls
Recalled Item: C2 CryoBalloon Focal Catheter Recalled by PENTAX of America Inc Due to The...
The Issue: The catheter alignment arrow printed onto the strain relief is not aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...
The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Automated Urine Chemistry System Recalled by Beckman Coulter...
The Issue: The Strip Provider Modules (SPM) on some of the instruments had not been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Functionality in the report sections "Findings Information" and "Summary of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...
The Issue: These one-way valves may disconnect at the joint between the two components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.