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. 2,716 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,716 in last 12 months

Showing 32813300 of 29,201 recalls

Medical DeviceJuly 31, 2024· Medtronic MiniMed, Inc.

Recalled Item: MiniMed 620G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2024· CooperSurgical, Inc.

Recalled Item: Silver-Plated Copper Sims Uterine Sound Recalled by CooperSurgical, Inc. Due...

The Issue: During the manufacturing process the devices were laser-marked with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2024· Medtronic MiniMed, Inc.

Recalled Item: MiniMed 630G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...

The Issue: During manufacturing, the last three tests from the 160 test flex of lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Agfa N.V.

Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...

The Issue: Potential for the front lever chain of the DR 800 table to fail.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing