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. 2,311 recalls have been distributed to South Dakota in the last 12 months.
Showing 38161–38180 of 47,632 recalls
Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...
The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE 46-SERIES Medical Washer-Disinfector Recalled by Getinge...
The Issue: Getinge Disinfection AB received complaints regarding sediment residuals in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dacarbazine Recalled by Hospira Inc. Due to Discoloration: Reconstituted...
The Issue: Discoloration: Reconstituted solution may appear pink instead of colorless...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...
The Issue: Lack of Assurance of Sterility; leaks were observed from the bag seam and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: While servicing a unit at a customer site, a field engineer discovered a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...
The Issue: A configuration update needs to be done on TactiSys to appropriately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer PERSONA Tibial Articular Surface Inserter Recalled by Zimmer, Inc....
The Issue: Potential for fracture of the tip of the product. The fractured tip is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoject E1 Fixed needle device Recalled by Owen Mumford USA, Inc. Due to...
The Issue: The syringe carrier is missing components: a damper and spring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BBL Port A Cul tubes Recalled by Becton Dickinson & Co. Due to The products...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL PT-Fibrinogen HS PLUS Recalled by Instrumentation Laboratory Co. Due...
The Issue: Some vials of HemosIL PT-Fibrinogen HS PLUS, Part No. 0008469810 (various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / Recalled...
The Issue: Accuray has become aware of a potential safety issue related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...
The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.