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. 1,041 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,041 in last 12 months

Showing 11701–11720 of 27,558 recalls

Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY CONN REDUCER 1/2 X 3/8 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY ASY STR CONN 3/8 STRLE 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY STR CONN 3/16 STRLE 24. REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 1/4 X 3/8 REDUCER W/LL 24. Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 3/8 STR CONN Recalled by LivaNova USA Inc. Due to The firm has identified...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ShockPulse-SE Lithotripsy System Recalled by Olympus Corporation of...

The Issue: A component of the Olympus ShockPulse Transducer was manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Philips North America, LLC

Recalled Item: ProxiDiagnost N90 Recalled by Philips North America, LLC Due to The thermo...

The Issue: The thermo switches in the three-phase transformer, which normally aid in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· LABORIE MEDICAL TECHNOLOGIES, CANADA ULC

Recalled Item: Pump Tube Set for MMS Libra and Solar Systems - Recalled by LABORIE MEDICAL...

The Issue: This field correction is being initiated to address potentially damaged...

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

Class II — Potential Health HazardOngoing