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. 2,520 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,520 in last 12 months

Showing 2046120480 of 50,591 recalls

DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Male+ Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Adipose Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2019· Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers

Recalled Item: Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail...

The Issue: Firm is recalling two lots of 2 lb. organic soybeans because they have the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 14, 2019· Mizuho OSI

Recalled Item: Levo Arm Label: LEVO ARM MIZUHO OSI Recalled by Mizuho OSI Due to Due to the...

The Issue: Due to the potential for fluid ingress into the Arm which could affect the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: Urine Electrolyte Diluent Recalled by Ortho Clinical Diagnostics Inc Due to...

The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: 7% BSA (Bovine Serum Albumin) Recalled by Ortho Clinical Diagnostics Inc Due...

The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Abbott Medical

Recalled Item: Radiofrequency Grounding Pad Recalled by Abbott Medical Due to Affected lots...

The Issue: Affected lots were manufactured with the protective release liner in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Becton Dickinson & Company

Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575...

The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2019· Becton Dickinson & Company

Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547...

The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...

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

Class II — Potential Health HazardOngoing
DrugOctober 11, 2019· X-Gen Pharmaceuticals Inc.

Recalled Item: Levetiracetam Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert - the incorrect package insert...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 11, 2019· TELEFLEX MEDICAL INC

Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...

The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2019· TELEFLEX MEDICAL INC

Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...

The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...

The Issue: The firm has become aware that there is a likelihood that a missing snap...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2019· LIFELINES NEURO COMPANY

Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...

The Issue: Potential for one of the four temporal electrode cables used in with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2019· LIFELINES NEURO COMPANY

Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...

The Issue: Potential for one of the four temporal electrode cables used in with the...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Sermorelin w/ GHRP2 3 mg For injection Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Chorionic Gonadotropin 11 Recalled by Innoveix Pharmaceuticals...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2019· Dollar General Corporation

Recalled Item: Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar Recalled by...

The Issue: Possible undeclared milk allergen in product.

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

Class II — Potential Health HazardOngoing
Refund