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Ziehm Imaging Inc Recall: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System.

Ziehm Imaging Inc Recall: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Ziehm Imaging Inc; Product: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging; Reason for recall: Engineer

Recalling firmZiehm Imaging Inc
ProductZiehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Reason for recallEngineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
ClassificationClass II (moderate — may cause temporary or reversible health consequences)
StatusTerminated
DistributionUSA (Nationwide) Distribution including the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MT, MA, MD, MI, MN, MN, MO,MS, NC ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Hawaii.
Recall initiated20131121
Recall numberZ-0565-2014
Categorydevice
StateFL
CountryUnited States

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