Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,360 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,360 in last 12 months

Showing 2604126060 of 27,558 recalls

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: 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: Goldvac(TM) UltraClean(R) Accessory Electrode 6 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: 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: 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: 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: 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 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 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
Medical DeviceDecember 21, 2012· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

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
Medical DeviceDecember 21, 2012· NordicNeuroLab AS

Recalled Item: nordicBrainEX Product Usage: nordicBrainEx is an image processing software...

The Issue: There is an error related to the relative geometry between fiber tracts in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Healthtronics, Inc.

Recalled Item: HealthTronics Endocare 3.8mm RenalCryo Cryoprobe Recalled by Healthtronics,...

The Issue: The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Concentric Medical Inc

Recalled Item: FlowGate Balloon Guide Catheter Recalled by Concentric Medical Inc Due to...

The Issue: Firm received complaints of resistance and possible collapse of the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Recalled by...

The Issue: A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Recalled by...

The Issue: Single needle packs in each case ( 10 needles per case) are mislabeled on...

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

Class II — Potential Health HazardOngoing