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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2102121040 of 47,632 recalls

DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: MOXIFLOXACIN 0.5% OPHTH SOLUTION SYRINGE Recalled by RXQ Compounding LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: ZINC SULFATE 1MG/ML INJECTION SOLUTION (PFV) Recalled by RXQ Compounding LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: DEXTROSE 50% INJECTION SOLUTION (PF) SYRINGE Recalled by RXQ Compounding LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: DEXPANTHENOL 250MG/ML (MDV) INJECTION SOLN Recalled by RXQ Compounding LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO DROPS (PHEN 0.625%/CYCLO 0.25%/TROP 0.25%/KETO 0.125%) OPHTH SOLN...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: CALCIUM CHLORIDE 100MG/ML (PFV) INJ SOLN Recalled by RXQ Compounding LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: EPHEDRINE 5MG/ML (PF) SYRINGE Recalled by RXQ Compounding LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: EPINEPHrine 4MG ADDED TO D5W 5% Recalled by RXQ Compounding LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: Avastin Recalled by RXQ Compounding LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: HYDROGEN PEROXIDE 3% INJECTABLE PFV Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: MOLYBDENUM 0.025MG/ML INJECTION SOLUTION Recalled by RXQ Compounding LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Elekta, Inc.

Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...

The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing