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. 2,386 recalls have been distributed to South Dakota in the last 12 months.
Showing 21301–21320 of 27,558 recalls
Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...
The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...
The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Scenaria Computed Tomography System Hitachi Medical Systems America...
The Issue: The firm discovered that the centrifugal force applied to the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...
The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic...
The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...
The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or Recalled by...
The Issue: When using the CIVCO biopsy attachments in combination with the ACUSON S...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...
The Issue: Potential missing segments on the display that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...
The Issue: Potential missing segments on the display that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter HomeChoice and HomeChoice Pro APD systems Recalled by Baxter...
The Issue: Loud operating sounds, which was unacceptable to the end users when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to The...
The Issue: The affected expired lots of product may have exhibited breakthrough growth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.