Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,041 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,041 in last 12 months

Showing 17261–17280 of 51,202 recalls

Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
DrugNovember 23, 2020· Ascend Laboratories LLC

Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories LLC Due to...

The Issue: Failed Impurity/Degradation Specifications: Unidentified impurities not...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor)...

The Issue: Labeling: Label mix-up

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 5 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 6 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 11 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· Complete Pharmacy and Medical Solutions, LLC.

Recalled Item: HUMAN CHORIONIC GONADOTROPIN 1 Recalled by Complete Pharmacy and Medical...

The Issue: CGMP deviations: Lack of potency testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2020· SCA Pharmaceuticals

Recalled Item: Fentanyl Recalled by SCA Pharmaceuticals Due to Subpotency:...

The Issue: Subpotency: Out-of-specification stability test result for low potency was...

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

Class III — Low RiskOngoing
Refund
FoodNovember 20, 2020· Riverside Natural Foods, Ltd.

Recalled Item: Good & Gather Banana Chocolate Chip Date & Nut Bars Recalled by Riverside...

The Issue: The product contains an undeclared almonds.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2020· Zimmer Biomet, Inc.

Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...

The Issue: Device has the potential for fracture during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...

The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Ortho-Clinical Diagnostics, Inc.

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...

The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Haag-Streit USA Inc

Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...

The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 11.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 12.5MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic Recalled by...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 16.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing