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. 2,150 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,150 in last 12 months

Showing 12611280 of 29,201 recalls

Medical DeviceJuly 17, 2025· Quest International, Inc.

Recalled Item: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant...

The Issue: Measles IgM Test Kit lacks premarket approval or clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...

The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System Bardex I.C. Complete Care Infection Control...

The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control...

The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2025· Philips Medical Systems (Cleveland) Inc

Recalled Item: Pinnacle 3 with TumorLOC Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: Due to software issue, Radiation Therapy Planning system may provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2025· PREMIA SPINE LTD

Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...

The Issue: Potential for missing pins at tip of inserter.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Prosthesis Head B Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Inconsistent size terminology and color coding used on labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2025· Stryker Communications

Recalled Item: Chromophare Surgical Light System Recalled by Stryker Communications Due to...

The Issue: Surgical lights have stress lines forming on the powder coating, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Plastic Trial Head Brown Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: Inconsistent size terminology and color coding used on labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic...

The Issue: Specific lots of reprocessed electrophysiology catheters may contain small...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Novum IQ Large Volume Pump Recalled by Baxter Healthcare Corporation...

The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 14, 2025· MAQUET GMBH

Recalled Item: Corin Operating Tables Model Numbers: (1) 770001A0 Recalled by MAQUET GMBH...

The Issue: Under certain conditions, such as the simultaneous use of the operating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2025· American Contract Systems Inc

Recalled Item: AMERICAN CONTRACT SYSTEMS Recalled by American Contract Systems Inc Due to...

The Issue: During an internal investigation, ACS determined that the rationale for...

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

Class II — Potential Health HazardOngoing