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 46614680 of 27,558 recalls

Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2024· Canon Medical System, USA, INC.

Recalled Item: Vantage Titan Recalled by Canon Medical System, USA, INC. Due to For some...

The Issue: For some MRI systems, it has been found that some of the maximum Spatial...

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

Class II — Potential Health HazardOngoing