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. 1,030 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,030 in last 12 months

Showing 15461–15480 of 47,632 recalls

DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...

The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...

The Issue: Microbial Contamination of Non-Sterile Product.Product is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· X-Gen Pharmaceuticals Inc.

Recalled Item: Neomycin Sulfate Tablets Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Failed Stability Specifications: Out of Specification (OOS) result reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to...

The Issue: Non-sterility.Product is being recalled because at labeled storage...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...

The Issue: CGMP Deviations: Product is being recalled because at labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...

The Issue: Non-sterility.Product is being recalled because at labeled storage...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...

The Issue: Microbial Contamination of Non-Sterile Product:.Product is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...

The Issue: CGMP Deviations: Product is being recalled because at labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...

The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Luminex Corporation

Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...

The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Gentueri Inc

Recalled Item: Gentueri Viral Transport Medium (VTM) Recalled by Gentueri Inc Due to Medium...

The Issue: Medium showed visual turbidity and discoloration, potentially contaminating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Coltene Whaledent Inc

Recalled Item: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Recalled by...

The Issue: The incorrect dental pins were packaged and subsequently distributed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Clark Laboratories, Inc.

Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....

The Issue: Positive Control may run high out of its assigned ISR range and result in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· SIGHT DIAGNOSTICS LTD

Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...

The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
FoodMarch 17, 2021· Real Water, Inc.

Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...

The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water

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

Class I — Serious Health HazardOngoing
Refund