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. 2,259 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,259 in last 12 months

Showing 4584145860 of 47,632 recalls

Medical DeviceSeptember 13, 2012· OrthoPediatrics Corp

Recalled Item: Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary...

The Issue: A complaint received from sales representative that a replenishment...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Heartsine Technologies, Limited

Recalled Item: HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501...

The Issue: Certain Samaritan 300/300P PAD devices may experience one or both of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Femoral Stem 12/14 Neck Taper Extended Offset Recalled by Zimmer, Inc....

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Modular Stem Recalled by Zimmer, Inc. Due to Zimmer Inc. is initiating a...

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· Zimmer, Inc.

Recalled Item: CPT Hip System Femoral Stem Petite Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2012· 3M Company - Health Care Business

Recalled Item: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac...

The Issue: 3M determined that the electrical grounding mechanism for the Steri-Vac 5XL...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Impurities/Degradation Products: An out of specification result for a known...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2012· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost with patient carriage Model: 712050 with serial...

The Issue: Hook does not securely hold the footplate in vertical position, causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Magnetom Skyra Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: When positioning the Flex Large 4 Coil (part No. 8625761) off-center in...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2012· Whole Foods Market

Recalled Item: Frescolina and Mitica brand Ricotta Salata cheeses were cut into wedges...

The Issue: Whole Foods Market announces that it is recalling ricotta salata sold in 21...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR Assay: Catalog Number: US: Recalled by Siemens...

The Issue: BR Assay for CA 27.29 Calibration Interval Change due quality control (QC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart XL M4735A Defibrillator/Monitors Recalled by Philips...

The Issue: HeartStart XL Defibrillator/Monitor (M4735A) used on a patient when AC power...

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

Class II — Potential Health HazardOngoing
DrugSeptember 10, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS Recalled by Vintage...

The Issue: Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 10, 2012· Forever Cheese Inc

Recalled Item: Marte brand Frescolina Ricotta Salata. Matured and packed by: Fattorie...

The Issue: Frescolina brand Ricotta Salata cheeses found positive for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 10, 2012· Invacare Corporation

Recalled Item: Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility...

The Issue: The potential exists for the wheel to rotate freely despite engagement of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: Recalled...

The Issue: Terumo Cardiovascular Systems (CVS) received two reports of the false back...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Polyaxial Screw...

The Issue: This action is being initiated following a detailed investigation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap...

The Issue: This action is being initiated following a detailed investigation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2012· Instrumentation Industries Inc

Recalled Item: Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators...

The Issue: Firm initiated an update to Directions for Use necessitating replacement of...

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

Class II — Potential Health HazardOngoing