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. 2,609 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,609 in last 12 months

Showing 1162111640 of 50,591 recalls

DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2022· WISSNER-BOSSERHOFF GMBH

Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...

The Issue: When the handset is disconnected from the power mains, and mains operation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2022· Synapse Biomedical Inc

Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG)...

The Issue: Due to a defect identified on the EPG controller printed circuit board...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2022· Intera Oncology, Inc.

Recalled Item: INTERA 3000 Hepatic Artery Infusion Pump Recalled by Intera Oncology, Inc....

The Issue: Higher than expected flow rate.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 7, 2022· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...

The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 7, 2022· OXFORD IMMUNOTEC LTD

Recalled Item: T-Cell Xtend .610 US Recalled by OXFORD IMMUNOTEC LTD Due to Due to...

The Issue: Due to equipment failure, affected products were stored at temperatures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· OXFORD IMMUNOTEC LTD

Recalled Item: T-SPOT.TB .300 US Recalled by OXFORD IMMUNOTEC LTD Due to Due to equipment...

The Issue: Due to equipment failure, affected products were stored at temperatures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· OXFORD IMMUNOTEC LTD

Recalled Item: AIM-V Medium .200/500 Recalled by OXFORD IMMUNOTEC LTD Due to Due to...

The Issue: Due to equipment failure, affected products were stored at temperatures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34033-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34032-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 34021-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 35001-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 32017-56 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 39421-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 81109-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2022· Chuckanut Bay Foods LLC

Recalled Item: Item 39417-12 Recalled by Chuckanut Bay Foods LLC Due to Undeclared Soy

The Issue: Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund