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. 2,266 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,266 in last 12 months

Showing 4304143060 of 47,632 recalls

Medical DeviceJuly 2, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...

The Issue: Upgrade installation script is designed to overwrite the same pouch files in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...

The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.

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

Class II — Potential Health HazardOngoing
DrugJuly 1, 2013· Fresenius Kabi USA, LLC

Recalled Item: Benztropine Mesylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of particulate matter: characterized as thin colorless flakes that...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...

The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Iradimed Corporation

Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...

The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Nata Komplete Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: NataChew Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS Recalled by Priester...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand FANCY ROASTED NUTS Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand NUTTY FAVORITES ASST Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath 4 Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's Fem-Vite Women's Anti-Oxidant Formula Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Fem-Vite was...

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

Class II — Potential Health HazardOngoing
Refund