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. 2,311 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,311 in last 12 months

Showing 3922139240 of 47,632 recalls

Medical DeviceSeptember 15, 2014· Primus Medical LLC

Recalled Item: AC Powered adjustable bed frame. AC powered adjustable bed frame Recalled by...

The Issue: Firm received several complaints that the head deck actuator bracket had...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System with Ventricular Catheter (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿¿ Systems HBc Total (HBcT) Kit. For In Vitro Recalled by...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

Class II — Potential Health HazardOngoing
DrugSeptember 15, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: TOPIRAMATE Tablets 200 mg Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2014· AbbVie Inc

Recalled Item: CREON (pancrelipase) Delayed-Release Capsules Recalled by AbbVie Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2014· Astellas Pharma US Inc

Recalled Item: Tarceva (erlotinib) Tablets Recalled by Astellas Pharma US Inc Due to Failed...

The Issue: Failed Dissolution Specifications: The product did not meet the acceptance...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 15, 2014· Gel Spice Co, Inc.

Recalled Item: Fresh Finds ground black pepper Net Wt. 3.53 oz (100g) Recalled by Gel Spice...

The Issue: Fresh Finds Black Pepper may contain Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 14, 2014· Invivo Corporation

Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...

The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...

The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured

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

Class III — Low RiskOngoing
Medical DeviceSeptember 12, 2014· Eyemart Express Ltd

Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...

The Issue: Prescription eyeglass safety lenses did not meet specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...

The Issue: The default for normal values are inconsistent between cobas b 221 and other...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2014· Intuitive Surgical, Inc.

Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...

The Issue: Correction due to the detection of a motor sensor failure in the Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...

The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2014· Expo Fresh L.L.C

Recalled Item: Roma Tomatoes Recalled by Expo Fresh L.L.C Due to Potential Salmonella...

The Issue: Expo Fresh is recalling Roma Tomatoes because they have a potential to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 11, 2014· Qualitest Pharmaceuticals

Recalled Item: MethylPREDNISolone TABLETS Recalled by Qualitest Pharmaceuticals Due to...

The Issue: Subpotent; 6 month stability time point

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

Class III — Low RiskOngoing
Refund
DrugSeptember 11, 2014· Hospira Inc.

Recalled Item: HEPARIN SODIUM Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: A particulate, confirmed as human hair, was...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 9, 2014· Hospira Inc.

Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specification: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2014· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...

The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: An endometrial suction curette is a device used to remove Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2014· Instrumed International, Inc.

Recalled Item: A circumcision clamp is an instrument used to compress the Recalled by...

The Issue: The reason these devices are being withdrawn from the market by Instrumed is...

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

Class II — Potential Health HazardOngoing