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. 2,534 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,534 in last 12 months

Showing 52615280 of 47,632 recalls

Medical DeviceMay 31, 2024· Zoll Medical Corporation

Recalled Item: ZOLL Powerheart G5 AED Recalled by Zoll Medical Corporation Due to G5...

The Issue: G5 Semi-Automatic AED is shipped, with a protective film over its front...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...

The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix MD - The Vertix MD Trauma has been Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size) Recalled by...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Single Patient Use (SPU) Circuit 5kit for Volara Recalled by...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Blue Ventilator Adapter Module. Intermittent positive...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing