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. 2,457 recalls have been distributed to Alabama in the last 12 months.
Showing 34381–34400 of 50,591 recalls
Recalled Item: Organic Stir-Fry Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...
The Issue: Organic Stir Fry is recalled because it has the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cut Green Beans Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...
The Issue: Green Beans are recalled because they have the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Supreme Bean & Carrot Blend Recalled by CRF Frozen Foods, LLC Due to...
The Issue: Bean & Carrot blend is recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Big House Blend Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...
The Issue: Mixed Vegetables are recalled because they have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peas & Carrots Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...
The Issue: Peas & Carrots are recalled because they have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mini Bow Tie Pasta and Vegetable Blend Recalled by CRF Frozen Foods, LLC Due...
The Issue: Mini Bow Tie Pasta and Vegetable Blend is recalled because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Root Medley Recalled by CRF Frozen Foods, LLC Due to Potential...
The Issue: Organic Root Medley is recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One...
The Issue: One of the dent markers from the DX-D600 dropped down from the overhead rail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...
The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.