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. 2,616 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,616 in last 12 months

Showing 1152111540 of 50,591 recalls

Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Corin Ltd

Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...

The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...

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

Class II — Potential Health HazardOngoing
DrugJuly 21, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: below specification limits for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: below specification limits for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2022· Ultra Supplement LLC

Recalled Item: SUSTANGO (Pendenadril Tytrate Blend) Capsules Recalled by Ultra Supplement...

The Issue: Marketed Without an Approved NDA/ANDA: Analytical testing showed the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 21, 2022· Cardiac Assist, Inc

Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...

The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 21, 2022· Medline Industries Inc.

Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...

The Issue: Due to a non-sterile component (tape) being place within the sterile portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2022· Getinge Usa Sales Inc

Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...

The Issue: Device does not meet regulatory requirements of stability while stationary,...

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

Class II — Potential Health HazardOngoing
DrugJuly 20, 2022· AVKARE Inc.

Recalled Item: Lamotrigine Tablets Recalled by AVKARE Inc. Due to Labeling: Label Error on...

The Issue: Labeling: Label Error on Declared Strength

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 20, 2022· Alcor Scientific, Inc.

Recalled Item: iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is Recalled by Alcor...

The Issue: Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto...

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

Class II — Potential Health HazardOngoing