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. 2,442 recalls have been distributed to South Dakota in the last 12 months.
Showing 18201–18220 of 27,558 recalls
Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...
The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...
The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....
The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raindrop Near Vision Inlay Recalled by Revision Optics Inc Due to ReVision...
The Issue: ReVision Optics has updated the instructions for use (IFU) for the Raindrop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.