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. 2,295 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,295 in last 12 months

Showing 441460 of 47,632 recalls

DrugDecember 16, 2025· SpecGx, LLC

Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...

The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) WCH...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 25GA I.D.D. Internal Delivery Device Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical Lindsell Sutured IOL Marker Recalled by Vortex Surgical Inc....

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical I2 Injection Kit Recalled by Vortex Surgical Inc. Due to...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Sysmex America, Inc.

Recalled Item: TS-10/TS-10H Tube Sorter Recalled by Sysmex America, Inc. Due to Under...

The Issue: Under specific conditions, the lift's electromagnetic holding force may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Hologic, Inc

Recalled Item: Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument....

The Issue: Presence of particulates in affected devices that can be deposited into...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Solo Precision IV Pump Recalled by ICU Medical, Inc. Due to...

The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Plum Duo Infusion Pump Recalled by ICU Medical, Inc. Due to Plum...

The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· Immunotech A.S.

Recalled Item: Estrone RIA Recalled by Immunotech A.S. Due to The affected Estrone RIA kit...

The Issue: The affected Estrone RIA kit lots may rarely give falsely high patient...

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

Class II — Potential Health HazardOngoing