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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2042120440 of 47,632 recalls

DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Club Pack Display Recalled by Medtech Products,...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Hand Pocket Pal Tray Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: HS70A Diagnostic Ultrasound System Version 2.01.00 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed...

The Issue: SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: WS80A Diagnostic Ultrasound System Version 1.00.16 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endintrak¿ 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac ECTR Push Blade Recalled by Stryker GmbH Due to The seal integrity...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing