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. 2,558 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,558 in last 12 months

Showing 1908119100 of 51,202 recalls

Medical DeviceApril 13, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product...

The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing