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. 1,090 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,090 in last 12 months

Showing 1601–1620 of 47,632 recalls

Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Baxter Healthcare Corporation

Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Greiner Bio-One North America, Inc.

Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...

The Issue: Blood collection tubes were manufactured with the label applied too high on...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2025· Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...

The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...

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

Class III — Low RiskOngoing
Medical DeviceAugust 6, 2025· Olympus Corporation of the Americas

Recalled Item: ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019....

The Issue: Potential for undetected, deformed a-traumatic tips.

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

Class I — Serious Health HazardOngoing
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH...

The Issue: Unapproved Drug Claims.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED PHYTOSTEROL 99%)...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild...

The Issue: Unapproved Drug Claims.

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

Class III — Low RiskOngoing
Refund