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. 2,452 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,452 in last 12 months

Showing 1480114820 of 47,632 recalls

Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Flowonix Medical Inc

Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...

The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Medline Industries Inc

Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...

The Issue: Potential for mold contamination (Aspergillus vadensis)

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...

The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...

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

Class II — Potential Health HazardOngoing
FoodMay 24, 2021· Hy-Vee Stores Inc

Recalled Item: Hy-Vee Chicken Street taco kit Recalled by Hy-Vee Stores Inc Due to...

The Issue: Product contains chipotle crema as part of a taco kit which contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 21, 2021· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide oil) 0.01% Ear Drops 20 mL bottles...

The Issue: Presence of Foreign Substance: Potential for broken glass within the glass...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 21, 2021· GE Healthcare, LLC

Recalled Item: CARESCAPE PDM-Masimo SpO2. Physiological data monitor. Recalled by GE...

The Issue: Masimo SpO2 Saturation Values can become frozen after an extended length of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Sunstar Americas, Inc.

Recalled Item: SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse Recalled by Sunstar Americas,...

The Issue: Products may be contaminated with micro-organisms Burkholderia cepacia...

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

Class II — Potential Health HazardOngoing