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. 2,638 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,638 in last 12 months

Showing 99019920 of 50,591 recalls

Medical DeviceFebruary 17, 2023· RAYSEARCH LABORATORIES AB

Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...

The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...

The Issue: Incorrect type of titanium was used which reduces the gripping strength of...

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2023· Azurity Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Azurity Pharmaceuticals, Inc....

The Issue: cGMP: complaints of crystals not redissolving into solution after warming...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2023· AVEVA Drug Delivery Systems, Inc.

Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...

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

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2023· AVEVA Drug Delivery Systems, Inc.

Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...

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

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2023· RISING PHARMACEUTICALS

Recalled Item: Warfarin Sodium Tablets Recalled by RISING PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2023· Foundation Medicine, Inc.

Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...

The Issue: An incorrect negative claim was identified on the claims page; the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· Merit Medical Systems, Inc.

Recalled Item: Flex-Neck Catheter External Repair Kit LOT CE-1400/A Recalled by Merit...

The Issue: Product that was built for design verification testing was inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2023· DePuy Orthopaedics, Inc.

Recalled Item: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM Recalled by...

The Issue: The subject product lots are being recalled because they received a higher...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2023· Nanomaterials Discovery Corporation

Recalled Item: Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer...

The Issue: Chemical Contamination: FDA analysis found the product to contain methanol,...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2023· Pharmedica USA, LLC

Recalled Item: Purely Soothing 15% MSM Drops Recalled by Pharmedica USA, LLC Due to...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2023· Pharmedica USA, LLC

Recalled Item: Purely Soothing MSM Nasal Spray Recalled by Pharmedica USA, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund