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. 2,481 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,481 in last 12 months

Showing 3596135980 of 51,202 recalls

DrugJanuary 21, 2016· Baxter Healthcare Corp.

Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: identified as a cloth fiber.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 20, 2016· Ouhlala Gourmet Llc

Recalled Item: Fruit Tartlets Recalled by Ouhlala Gourmet Llc Due to Undeclared Milk

The Issue: Products contain undeclared milk on finished product labeling

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 20, 2016· Ouhlala Gourmet Llc

Recalled Item: Fruit Tartlets Recalled by Ouhlala Gourmet Llc Due to Undeclared Milk

The Issue: Products contain undeclared milk on finished product labeling

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 20, 2016· Zimmer Biomet, Inc.

Recalled Item: Herga foot switch Recalled by Zimmer Biomet, Inc. Due to Complaints were...

The Issue: Complaints were received reporting the system would freeze/shut down while...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Magellan Diagnostics, Inc.

Recalled Item: LeadCare II Blood Lead Test Kit Recalled by Magellan Diagnostics, Inc. Due...

The Issue: LeadCare II Test Kits controls out of range

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· AGFA Healthcare Corp.

Recalled Item: AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for...

The Issue: The DX-D100 User Manual already contained information about to move a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2016· Integrated Medical Systems Inc

Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...

The Issue: If excessive pressure is applied to the distal end of the endoscope, the...

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

Class II — Potential Health HazardOngoing