Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,733 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,733 in last 12 months

Showing 4654146560 of 49,150 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: 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: Goldvac(TM) UltraClean(R) Accessory Electrode 6 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: 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· 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: UltraClean(R) Accessory Electrode 1 inch Coated Needle 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 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: Electrosurgical Tip Cleaner Recalled by ConMed Corporation Due to 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 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: 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· 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: 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: 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· 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: 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: 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
DrugDecember 22, 2012· D& S Herbals, LLC

Recalled Item: Super Power capsules Recalled by D& S Herbals, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: This dietary supplement has been...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.45 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.9 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund