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. 2,456 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,456 in last 12 months

Showing 1580115820 of 27,558 recalls

Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROW JACC with Chlorag+ard Technology Recalled by Arrow International Inc...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWgard Blue¿ Sheath and Integral...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Two-Lumen CVC Kit Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Echogenic Introducer Needle Recalled by Arrow International Inc Due to...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ PSI Kit with Integral Hemostasis Valve/ Side Port Recalled...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Clear Fenestrated Drape with Adhesive Recalled by Arrow International Inc...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROW PICC Set Recalled by Arrow International Inc Due to Product sterility...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Recalled by Arrow International Inc...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Catheter Hemostasis Valve For use with .038" (.096 cm) dia. Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWgard Blue PLUS¿ Multi-Lumen CVC Kit with Blue FlexTip¿ Catheter...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: 9 Fr. Radiopaque Polyurethane Sheath/Dilator with Integral Hemostasis...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Spring Wire Guide Introducer Needle Recalled by Arrow International Inc Due...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing