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. 1,060 recalls have been distributed to South Dakota in the last 12 months.
Showing 9621–9640 of 27,558 recalls
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed Visions PV .035 IVUS Catheter Recalled by Northeast...
The Issue: 510k indicated one (1) reprocessing cycle, product not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...
The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centaur Syphilis Assay-SYP Kit Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for the ADVIA Centaur Syphilis assay to carryover into other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...
The Issue: Removing parts for safety reasons due to possible breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPTAR Laser Range Finders Recalled by Potomac River Group, Corp. Due to...
The Issue: RAPTAR units are capable of being field modified to enable the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for...
The Issue: One batch of the ELUVIATM Drug Eluting Vascular Stent System incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.