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 15321–15340 of 47,632 recalls

DrugMarch 26, 2021· Antoto-K

Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· Cosette Pharmaceuticals, Inc.

Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...

The Issue: CGMP Deviaitons

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Moisture Limits: Out of specification for water content

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

Class III — Low RiskOngoing
Refund
DrugMarch 25, 2021· Namoo Enterprise LLC

Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· S & B Story LLC

Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Model Number: (9A)9.0.0.113 Recalled by RAYSEARCH LABORATORIES AB...

The Issue: Flags edited in RayCare after a patient has been checked in may not always...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas SARS-CoV-2 & Influenza A/B assay cobas Liat- Reagents Recalled by...

The Issue: Invalid or false positive results for one or more targets...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas Liat Analyzer: respiratory virus panel nucleic acid assay system...

The Issue: Invalid or false positive results for one or more targets...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVPlasty Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G SINGLE CEMENT DELIVERY KIT (5 FILLERS). For use in Recalled by Zavation...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Unipedicular Cement Delivery Cannula Kit Recalled by Zavation Due...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Directional Cement Cannula (4 pieces per pack) Recalled by Zavation...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing