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. 2,465 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,465 in last 12 months

Showing 1532115340 of 27,558 recalls

Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER TRAY Recalled by Medical...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Double Lumen CRRT/ABP Catheter Set Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow IJ Full Tray Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Folate Reagent Pack(10758750009237)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· GE Healthcare, LLC

Recalled Item: Revolution CT systems with the SmartStep Option The system is Recalled by GE...

The Issue: On the Revolution CT systems equipped with the SmartStep Option, the Z...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Prolactin Reagent Pack (10758750000111)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...

The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Merit Medical Systems, Inc.

Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...

The Issue: A nonsterile bulk product designated for further processing in a tray was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing