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 4224142260 of 47,632 recalls

Medical DeviceSeptember 24, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Soft Tissue Retractor Small Extendible Offset blade facilitates easy...

The Issue: The potential exists for the locking screw nut to break on the Soft Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Baxter Healthcare Corp.

Recalled Item: SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP...

The Issue: Baxter Healthcare Corporation is recalling the LCD display screen on the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 24, 2013· Hospira Inc.

Recalled Item: Metoclopramide Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Potential vendor glass issue - glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2013· Hospira Inc.

Recalled Item: Ondansetron Injection Recalled by Hospira Inc. Due to Presence of Particular...

The Issue: Presence of Particular Matter: Potential vendor glass issue - glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2013· W.S. Badger Company Inc.

Recalled Item: Badger Kids Broad Spectrum SPF30 Zinc Oxide Sunscreen Lotion Tangerine &...

The Issue: Microbial Contamination of Non-Sterile Products; Selected lots of Badger...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2013· W.S. Badger Company Inc.

Recalled Item: Badger Baby Broad Spectrum SPF 30 Zinc Oxide Sunscreen Lotion Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products; Selected lots of Badger...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· Watson Laboratories Inc

Recalled Item: Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet)...

The Issue: Failed Tablet/Capsule Specifications: Multiple complaints for push through...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· Tolmar, Inc.

Recalled Item: Ketoconazole Shampoo Recalled by Tolmar, Inc. Due to Subpotent

The Issue: Subpotent

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2013· Volcano Corp

Recalled Item: ComboMap Intravascular Flow and Pressure System Recalled by Volcano Corp Due...

The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 26g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 22g Quincke (Without Introducer)...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs  25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Baylis Medical Corp *

Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...

The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g/25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing