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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 27261–27280 of 27,558 recalls
Recalled Item: Vector TAS Modular Driver Recalled by Ormco/Sybronendo Due to The...
The Issue: The Instructions For Use (IFUs) for Vector TAS Modular Driver for some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)...
The Issue: Some of the sterile packages had broken seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone. The PrepStain System is...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Slide Processor. The PrepStain System is a liquid-based thin...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain PM Kit Recalled by Tripath Imaging, Inc. Due to Some Prep Stain...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a Recalled by Tripath...
The Issue: Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry...
The Issue: The recall was initiated because Sunquest has confirmed that the Sunquest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSX-IOI: AQUILION 32/64 Recalled by Toshiba American Medical Systems Inc Due...
The Issue: The firm initiated this recall due to a potential software issue. The DLP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: RX Accunet Embolic Protection System Common Name: RX Recalled by...
The Issue: The recall was initiated because Abbot Vascular has discovered that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA INFINITY MR SYSTEM WITH EXCITE TECHNOLOGY GE 3.0T SIGNA Recalled by GE...
The Issue: Screen save images are included in wrong exam due to duplicate UID creation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom Cordless LED Light System. Freedom System Recalled by Kerr...
The Issue: The firm recalled the Freedom Cordless LED Headlight because some units were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory : intended for use by professionals working in Recalled...
The Issue: Online calculations may not be performed as expected or may yield results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic retrieval device. The disposable Raptor grasping device in...
The Issue: When the outer catheter is either coiled or in a contorted configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Recalled by Biomet 3i, LLC Due to On November 3, 2011 Biomet 3i,...
The Issue: On November 3, 2011 Biomet 3i, Palm Beach Gardens, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory Recalled by Sunquest Information Systems, Inc. Due to...
The Issue: Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.7/1.2JG326D-265 Product Usage: The device is a mobile X-ray system...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.7/1.3U163CS-36 In combination with below systems MobileArt Evolution...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.4/0.7JG326D-265AX/AT Product Usage: The device is a mobile X-ray system...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-20J Recalled by Shimadzu Medical Systems Due to Shimadzu is recalling...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.7U163CS-36 In combination with below systems MUX-100H Recalled by Shimadzu...
The Issue: Shimadzu is recalling Diagnostic X-ray Beam-Limiting Device, Mobile x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.