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. 2,259 recalls have been distributed to South Dakota in the last 12 months.
Showing 47601–47620 of 47,632 recalls
Recalled Item: 5.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Tulip Recalled by NuVasive Inc Due to The tulip portion of the screw...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. Recalled by...
The Issue: GE initiated a correction to the instructions/use due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...
The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory...
The Issue: Distribution of a product that did not meet specifications. (labeling error)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navitrack¿ System - OS Knee Universal Recalled by Orthosoft, Inc. dba Zimmer...
The Issue: ZIMMER CAS voluntarily conducted a retrospective recall of the Navitrack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS Recalled by...
The Issue: Ventana Medical System is initiating the recall of the BenchMark and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: popchips¿ Sea Salt & Vinegar Recalled by Sonora Mills Foods Due to The firm...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheddar Mini Rice Snacks under the following brand names: Fred Meyer...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: popchips¿ Cheddar Potato Recalled by Sonora Mills Foods Due to The firm...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TSX-301A/2 Aquilion One CT System. The TSX-30IAl2 is a whole Recalled by...
The Issue: The SureStart function may not operate in the usual manner, and you may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXCELART Vantage Recalled by Toshiba American Medical Systems Inc Due to The...
The Issue: The status display in the sequence queue window may not change from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Impactor - Dorado IBC Recalled by SpineFrontier, Inc. Due to During...
The Issue: During two separate occasions an impactor plate on the handle broke off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To...
The Issue: The outer jacket is receding away from the black sensor prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT Link Waterbath Recalled by Dako North America Inc. Due to Dako is...
The Issue: Dako is recalling the PT Link Waterbath because of a possible electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba CT systems Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: The systems all have a similar table control board. It has been found that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics...
The Issue: The power to the Esprit Display's Backlight is interrupted, causing the GUI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HiRes 90K devices with Helix Electrodes Model CI 1400-02H The Recalled by...
The Issue: Advanced Bionics is recalling the the HiRes 90K cochlear implant with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leflunomide tablets Recalled by Apotex Corp. Due to Subpotent (Single...
The Issue: Subpotent (Single Ingredient Drug): Distribution of product that did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.