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. 2,295 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,295 in last 12 months

Showing 4064140660 of 47,632 recalls

FoodMarch 26, 2014· Oscar's Hickory House, Inc.

Recalled Item: OSCAR'S SMOKE HOUSE PLAIN CHEDDAR SPREAD Recalled by Oscar's Hickory House,...

The Issue: Products were recalled due to potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 26, 2014· Acumed LLC

Recalled Item: The Osteo-Clage System consists of stainless steel cable/sleeves and...

The Issue: Manufacturing of these devices with a grade of stainless steel that is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Specialty Diluent Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2014· Acumed LLC

Recalled Item: The Acumed Tension Band Pin is a fixation pin which Recalled by Acumed LLC...

The Issue: Certain lots of Acumed Tension Band Pins are being recalled because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products FS Diluent Pack 3 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2014· Branan Medical Corporation

Recalled Item: ToxCup Drug Screen Cup Recalled by Branan Medical Corporation Due to May be...

The Issue: May be labeled with incorrect result interpretation graphics on the ToxCup...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker PenAdapt" Recalled by Stryker Instruments Div. of Stryker...

The Issue: During packaging verification testing, a failure occurred due to cuts in the...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2014· First Aid Only Inc

Recalled Item: Smart Tab First Aid ezRefill System Ibuprofen dispenser boxes (Item Recalled...

The Issue: First Aid Only, Inc is recalling Smart Tab First Aid ezRefill System...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2014· Hospira Inc.

Recalled Item: Demerol Recalled by Hospira Inc. Due to Labeling; Missing label; ampoules...

The Issue: Labeling; Missing label; ampoules are missing the immediate container label

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

Class III — Low RiskOngoing
Refund
FoodMarch 25, 2014· Magno Humphries Laboratories, Inc

Recalled Item: OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product...

The Issue: Magno Humphries Laboratories is recalling Vitamin E softgels because the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Hospira Inc.

Recalled Item: LATEX-FREE Recalled by Hospira Inc. Due to The Tyvek cover may not be...

The Issue: The Tyvek cover may not be completely sealed to the rest of the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· AlloSource, Inc.

Recalled Item: AlloFuse DBM Putty 5cc Recalled by AlloSource, Inc. Due to The donor was...

The Issue: The donor was hemodiluted.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate Cat No. 06891541 SMN 10325366 (500 Recalled by...

The Issue: Serum controls may go out of range low with the ADVIA Centaur ¿Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2014· Draeger Medical, Inc.

Recalled Item: Reusable latex breathing bags with multiple part numbers and sold Recalled...

The Issue: Reusable latex breathing bags with various part numbers and sold as part of...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2014· Apotex Inc.

Recalled Item: Paroxetine HCL Controlled-Release Tablets 25 mg Recalled by Apotex Inc. Due...

The Issue: Chemical Contamination: Product were manufactured with active pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2014· Apotex Inc.

Recalled Item: PAXIL (Paroxetine HCL) Tablets 40 mg Recalled by Apotex Inc. Due to Chemical...

The Issue: Chemical Contamination: Product were manufactured with active pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund