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Recall Observatory FDA recall evidence

Device product

Hydra Vision DR 60/80 System, Models 700539 and 700540, Liebel-Flarshiem Company. The System is used in radiologic imaging procedures.

Z-1753-2013

April 25, 2013

Class II

Product summary

Firm
Leibel-Flarsheim Company LLC
Event
Event 65176
Status
Terminated
Classification
Class II
Quantity
12 units
Official record key
device-enforcement:Z-1753-2013

Official wording

Reason: A complaint was received in which a hospital physicist indicated the dosage was too high on the HUT system. During the service call the systems Maximum Fluoro Dose was found to be 30 R/min which is three times the Maximum Fluoro Dose limit of 10 R/min.

Code information: The following catalog numbers, serial numbers and associated manufacturing dates are affected by this recall: 700539 CI0807H273 August2007; 700539 CI0106H162 January 2006; 700539 CI1010H523 October 2010; 700539 CI0811H567 August 2011; 700539 CI0108H313 January 2008; 700539 CI0309H418 March 2009; 700539 15031229 Apri12003; 700539 14031227 Apri12003; 700539 CI0404H045 January 2005; 700539 CI0504H054 May 2004; 700539 CI1106H208 November 2006; 700539 CI0509H424 May 2009

Distribution pattern: Nationwide Distribution (US), including the states of TN, KY, CO, KS, CT, HI, and AZ.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    A complaint was received in which a hospital physicist indicated the dosage was too high on the HUT system. During the service call the systems Maximum Fluoro Dose was found to be 30 R/min which is three times the Maximum Fluoro Dose limit of 10 R/min.