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. 2,642 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,642 in last 12 months

Showing 83818400 of 50,591 recalls

DrugJuly 14, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: CARDIOPLEGIA SOLUTION Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of assurance of sterility. Validation data for decontamination cycles...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 14, 2023· Quest Medical, Inc.

Recalled Item: Q2 Multiport Extension set Recalled by Quest Medical, Inc. Due to For...

The Issue: For administration of intravenous fluids to a patient s vascular system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: MobileLink Acetabular Cup System Recalled by Waldemar Link GmbH & Co. KG...

The Issue: Product is labeled with incorrect offset.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Instrumentation Laboratory

Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...

The Issue: Sample misidentification could occur under specific conditions and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· EMPATICA SRL

Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...

The Issue: May have a battery life lasting less than the full 48 hours, requiring the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...

The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...

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

Class II — Potential Health HazardOngoing
DrugJuly 13, 2023· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate-Testosterone Propionate 180-20 mg/mL in cottonseed...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 13, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Methylphenidate Hydrochloride Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Presence of Foreign Substance: Metal embedded in a tablet.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2023· Medtronic Sofamor Danek USA, Inc

Recalled Item: CD HORIZON Spinal System Solera Awl Tip Tap Recalled by Medtronic Sofamor...

The Issue: Incorrect Laser Marking - Solera Awl Tip Tap

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 2 Readers Recalled by Abbott Diabetes Care, Inc. Due to If...

The Issue: If blood glucose monitoring system users attempt to start a new sensor, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing