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. 2,413 recalls have been distributed to Alabama in the last 12 months.
Showing 42981–43000 of 50,591 recalls
Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...
The Issue: Surface finish is different than specified. The implant has 30 grit blast on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...
The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis TEARS Recalled by Oasis Medical Inc Due to Labeling: Missing Label;...
The Issue: Labeling: Missing Label; The label on the immediate bottle is missing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MicroScan -Neg Breakpoint Combo Panel Type 34 Recalled by Beckman Coulter,...
The Issue: Siemens Healthcare Diagnostics has received complaints regarding panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.