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. 2,447 recalls have been distributed to South Dakota in the last 12 months.
Showing 17301–17320 of 27,558 recalls
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...
The Issue: Penumbra has identified an issue in these four lots involving a raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...
The Issue: Identification of excess plastic on the tip of the cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect diabetes management software app Recalled by Roche...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.