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FDA Device recall Z-2833-2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedur…

On 2018-08-29 the FDA classified a Class II recall of Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedur… by Liebel Flarsheim, citing software issue. The difference between the display and dosimeter readings In the Child/Pediatric automatic exposure mode is in the range of 52-65%. The display in all other modes….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2833-2018
ClassificationClass II
Statusterminated
Initiated2017-02-27
Published2018-08-29
Last updated2026-09-13 11:54 UTC
CompanyLiebel Flarsheim
DistributionAL, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, MD, MI, MN, NC, NH, NV, NY, OH, OK, PA, SC, TN, TX, VA, WA, WI, WV

Product

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requiring a beam of diagnostic quality radiation, primarily for urological applications such as functional x-ray diagnostics, endourology and minimal invasive urology/ surgery.

Reason

Software issue. The difference between the display and dosimeter readings In the Child/Pediatric automatic exposure mode is in the range of 52-65%. The display in all other modes deviated by less than 35% from the dosimeter readings.

Identifiers

code_infoProduct ID : 750732 SHF-635RF, 750733 SHF-835RF

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2833-2018%22

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