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. 1,061 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,061 in last 12 months

Showing 15981–16000 of 51,202 recalls

DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFELX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Sodium Chloride 0.9% Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 28, 2021· Randox Laboratories Ltd.

Recalled Item: Randox RX Imola Analyser with ISE Recalled by Randox Laboratories Ltd. Due...

The Issue: An issue was identified where the software froze during processing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II...

The Issue: Incorrect stentstop assembly (18fr) was used to build the delivery system...

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

Class II — Potential Health HazardOngoing
FoodApril 28, 2021· NOW Health Group Inc.

Recalled Item: NOW 4x6 Acidophilus Recalled by NOW Health Group Inc. Due to Undeclared...

The Issue: Foreign capsules included in bottle. Undeclared ingredients.

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

Class III — Low RiskOngoing
Refund
FoodApril 27, 2021· Brill Inc

Recalled Item: 10239710: 12" BAKED CHOCOLATE CHIP MESSAGE COOKIE 14 / 22 Recalled by Brill...

The Issue: Potential to contain small foreign objects

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 27, 2021· PUBLIC GOODS

Recalled Item: PUBLIC GOODS brand HAIR Recalled by PUBLIC GOODS Due to Undeclared Soy

The Issue: Product may contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 27, 2021· Brill Inc

Recalled Item: 10233579 JUMBO CHOCOLATE CHIP COOKIE 12 / 12 INCH BAKED Recalled by Brill...

The Issue: Potential to contain small foreign objects

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 27, 2021· Brill Inc

Recalled Item: 10194739 TranSmart" 12 INCH CHOCOLATE CHIP MESSAGE COOKIE 24/24 OUNCE...

The Issue: Potential to contain small foreign objects

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 27, 2021· Quanta System, S.p.A.

Recalled Item: Quanta System Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A....

The Issue: Product sterility is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Quanta System, S.p.A.

Recalled Item: Olympus Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A. Due to...

The Issue: Product sterility is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Quidel Corporation

Recalled Item: Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent Recalled by...

The Issue: In rare situations patients infected with high viral load of SARS CoV 2 may...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2021· Circulatory Technology Inc.

Recalled Item: The Better-Bladder (BB) Recalled by Circulatory Technology Inc. Due to The...

The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Quanta System, S.p.A.

Recalled Item: Quanta System Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A....

The Issue: Product sterility is potentially compromised.

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

Class II — Potential Health HazardOngoing