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. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2760127620 of 29,201 recalls

Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Needle with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· Heartware Inc

Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...

The Issue: HeartWare, Inc. of Miami Lakes, FL is recalling their Ventricular Assist...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode Recalled by ConMed Corporation Due to...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ABC(R) NOZZLE Recalled by ConMed Corporation Due to ConMed received...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 1 inch Coated Blade with...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· Stryker Spine

Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...

The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: CONMED(R) ELECTROSURGICAL SAFETY HOLSTER Recalled by ConMed Corporation Due...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: TUR/Endoscopic Cable Recalled by ConMed Corporation Due to ConMed received...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ELECTROSURGICAL ENT NEEDLE ELECTRODE Recalled by ConMed Corporation Due to...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 25, 2012· bioMerieux, Inc.

Recalled Item: BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle...

The Issue: BacT/ALERT SA Culture Bottle lot 1031866 may contain bottles with uncured...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE MOIST Brand Contact Lenses Recalled by Johnson & Johnson Vision...

The Issue: Limited number of individual contact lens packages may not have been...

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

Class II — Potential Health HazardOngoing