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. 2,589 recalls have been distributed to Alabama in the last 12 months.
Showing 15621–15640 of 50,591 recalls
Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirolimus Tablets 1 mg Recalled by American Health Packaging Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera Recalled by...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipodrene With 25mg Ephedra Extract 100CT Recalled by Hi Tech...
The Issue: The firm was notified by the FDA that the product contains the unapproved...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.