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. 2,260 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,260 in last 12 months

Showing 4508145100 of 47,632 recalls

Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 4, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...

The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...

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

Class I — Serious Health HazardOngoing
DrugJanuary 3, 2013· Mobius Therapeutics LLC

Recalled Item: Mitosol (mitomycin for solution) Recalled by Mobius Therapeutics LLC Due to...

The Issue: Non-Sterility: one or more components of the kit have been found to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2013· Animas Corporation

Recalled Item: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is Recalled...

The Issue: Animas has identified a component issue affecting a small supply of the...

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

Class I — Serious Health HazardOngoing
FoodJanuary 2, 2013· EonNutra, LLC

Recalled Item: Growth Factor Complex 200 GFC 200 Recalled by EonNutra, LLC Due to Eon...

The Issue: Eon Nutra, LLC is recalling certain SOTO Supplements GFC 200 because the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 2, 2013· Lumenis Limited

Recalled Item: The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for...

The Issue: Lumenis Ltd is recalling certain models of VersaCut Morcellator devices to...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 31, 2012· Diagnostic Hybrids Inc

Recalled Item: Diagnostic Hybrids Recalled by Diagnostic Hybrids Inc Due to RhMK product...

The Issue: RhMK product fungal contamination.

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

Class III — Low RiskOngoing
DrugDecember 28, 2012· Advance Pharmaceutical Inc

Recalled Item: Rugby NATURAL IRON SUPPLEMENT Ferrous Sulfate Recalled by Advance...

The Issue: Labeling; Label Mixup; bottles of Ferrous Sulfate actually contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2012· Hillyard GMP

Recalled Item: HILLYARD Recalled by Hillyard GMP Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: The product may be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2012· Veridex, LLC

Recalled Item: CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage:...

The Issue: Veridex, LLC has received a report that a patient's demographics were...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2012· Veridex, LLC

Recalled Item: CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage:...

The Issue: Veridex, LLC has received a report that a patient's demographics were...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2012· Beckman Coulter Inc.

Recalled Item: Creatinine Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...

The Issue: Beckman Coulter is including additional information and instructions in the...

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

Class II — Potential Health HazardOngoing
DrugDecember 27, 2012· Ranbaxy Inc.

Recalled Item: Lac-Hydrin (ammonium lactate) Lotion Recalled by Ranbaxy Inc. Due to...

The Issue: Crystallization: Recall is due to a non-characteristic gritty/sandy texture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 27, 2012· Ranbaxy Inc.

Recalled Item: Lac-Hydrin (ammonium lactate) Cream Recalled by Ranbaxy Inc. Due to...

The Issue: Crystallization: Recall is due to a non-characteristic gritty/sandy texture...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 27, 2012· Heartware Inc

Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...

The Issue: HeartWare, Inc. of Miami Lakes, FL is recalling their Ventricular Assist...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· Stryker Spine

Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...

The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...

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 1 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 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 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