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. 1,670 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,670 in last 12 months

Showing 4218142200 of 47,632 recalls

FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Original Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Everything Net Wt. 9.6 oz (272 Recalled by R.A.B....

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Garlic Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Unsalted Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 1, 2013· R.A.B. Food Group LLC

Recalled Item: Tam Tams Snack Crackers Onion Net Wt. 9.6 oz (272 Recalled by R.A.B. Food...

The Issue: The Manischewitz Company, Newark, NJ is recalling various Tam Tam Products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
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· 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 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· 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· 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 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· 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· 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· 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· 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· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM 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 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