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. 2,365 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,365 in last 12 months

Showing 2460124620 of 27,558 recalls

Medical DeviceOctober 2, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Recalled by Stryker Instruments Div. of Stryker Corporation Due to It was...

The Issue: It was discovered that the silicone potting failed to properly cure after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2013· Nipro Diagnostics, Inc.

Recalled Item: MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for...

The Issue: Manufactured with an incorrect factory set unit of measure.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe Warmer Recalled by GE Healthcare, LLC Due to Oxygen...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· Toshiba American Medical Systems Inc

Recalled Item: TSX-101A Aquilion 32/64 ONE Computed Tomography X-Ray System Recalled by...

The Issue: Toshiba intitiated this recall because their investigation revealed that due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· Helix Medical LLC

Recalled Item: Blom-Singer Adjustable Tracheostoma Valve II Models: BE8025H and BE8025H-R3...

The Issue: InHealth Technologies (IHT) is recalling the Blom-Singer Adjustable...

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

Class III — Low RiskOngoing
Medical DeviceOctober 1, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker...

The Issue: Stryker received a report from the field indicating that a 5.5 mm Cancellous...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe and Panda Bag and Mask Resuscitation System Recalled...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe¿ and Panda¿ iRes Infant Warmer Product Recalled by...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2013· Merit Medical Systems, Inc.

Recalled Item: Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine...

The Issue: Custom Procedural Trays/Kits contain 1% Lidocaine HCl injection which were...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2013· Ethicon Endo-Surgery Inc

Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...

The Issue: During aging studies, the firm determined that the gastric belts were unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Ethicon Endo-Surgery Inc

Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...

The Issue: During aging studies, the firm determined that the gastric belts were unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Recalled by...

The Issue: A potential non conformance was identified with the Zero-P VA plate where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Bard Peripheral Vascular Inc

Recalled Item: Bard LifeStent Solo Vascular Stent Recalled by Bard Peripheral Vascular Inc...

The Issue: Bard Peripheral Vascular is recalling specific lots of Bard Lifestent Solo...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Ethicon Endo-Surgery Inc

Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...

The Issue: During aging studies, the firm determined that the gastric belts were unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Draeger Medical, Inc.

Recalled Item: Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended Recalled by...

The Issue: Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM Recalled...

The Issue: Stryker has received complaints associated with cracks and/or fracture of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified customers regarding over stimulation or stimulation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified customers regarding over stimulation or stimulation in...

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

Class II — Potential Health HazardOngoing