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. 2,273 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,273 in last 12 months

Showing 4240142420 of 47,632 recalls

Medical DeviceSeptember 10, 2013· Baxter Healthcare Corp.

Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...

The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Integra Limited

Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...

The Issue: Integra LifeSciences has identified through an internal evaluation that in...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Bevacizumab 1.25 mg/0.05 mL PF Recalled by Avella of Deer Valley, Inc. Due...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Beckman Coulter Inc.

Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...

The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...

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

Class II — Potential Health HazardOngoing