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. 2,295 recalls have been distributed to South Dakota in the last 12 months.
Showing 41221–41240 of 47,632 recalls
Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...
The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15%...
The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9%...
The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...
The Issue: Failed Tablet/Capsule Specifications: Split tablets were found in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...
The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...
The Issue: There is a potential for communication loss associated with the F5-01 Frame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...
The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...
The Issue: Potential for unexpected heating of the transformer mounting bolt located...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINERAL IV Injection Recalled by Abrams Royal Pharamacy Due to...
The Issue: Non-Sterility; analytical results found product to contain Sphingomonas...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...
The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that the outer shipping package for one lot (Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...
The Issue: Three problems were reported to the firm: When positioning for a relative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...
The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...
The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.