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. 2,483 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,483 in last 12 months

Showing 2484124860 of 50,591 recalls

DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: CeraVe Healing Lip Balm/SPF 30 (avobenzone 3% Recalled by Product Quest...

The Issue: Microbial Contamination of Non-Sterile Products: Failed microbiological...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: CVS Health Recalled by Product Quest Manufacturing LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: OCEAN Saline Nasal Spray Recalled by Product Quest Manufacturing LLC Due to...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: Premier Value Recalled by Product Quest Manufacturing LLC Due to Superpotent...

The Issue: Superpotent Drug: high out of specification assay results for the menthol...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: Rhinall Nasal Decongestant Nasal Spray (phenylephrine HCl) Recalled by...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2018· Product Quest Manufacturing LLC

Recalled Item: CVS Health Recalled by Product Quest Manufacturing LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions that could impact...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 4000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Ipamorelin 9 mg vial Lyophilized 1109 East Hallandale Beach Blvd. Recalled...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Ipamorelin 3 mg Lyophilized 1 vial 1109 East Hallandale Beach Recalled by...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Methylcobalamin 10 mg vial Lyophilized 1109 East Hallandale Beach Blvd....

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
DrugAugust 2, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications - OOS was observed for ATV...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 20000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 6000 IU Vial Lyophilized 1109 East Hallandale...

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
Medical DeviceAugust 2, 2018· Acumedia Manufacturers, Inc.

Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...

The Issue: Expiration date on the label is incorrect. Correct expiration date was...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...

The Issue: The implant only has one bolt in the sterile package but it should have had two.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...

The Issue: The implant only has one bolt in the sterile package but it should have had two.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· COVIDIEN LLC

Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...

The Issue: Potential for product sterility breach due to a compromised or pinched seal...

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

Class II — Potential Health HazardOngoing