RecallRadar

FDA Device recall Z-0391-2017

OR Table, Top U26 H V, Model # 1909793

On 2016-11-16 the FDA classified a Class II recall of OR Table, Top U26 H V, Model # 1909793 by Trumpf Medical Systems, citing trumpf has identified six incidents of pinched cables.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0391-2017
ClassificationClass II
Statusterminated
Initiated2016-10-25
Published2016-11-16
Last updated2026-09-13 11:54 UTC
CompanyTrumpf Medical Systems
DistributionUS

Product

OR Table, Top U26 H V, Model # 1909793; OR Table Top U26 H V U, Model # 1909794; OR Table Top U24 H V, Model # 1909796; OR Table Top U24 H V U, Model # 1909797; OR Table Top U24 H V W, Model # 1909798; OR Table Top U14 H V, Model # 1909799 Product Usage: Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Patient transport on the operating table top from a patient transfer system to the operating theater or from the operating theater to a patient transfer system.

Reason

Trumpf has identified six incidents of pinched cables.

Identifiers

code_info
Model # 190973 - Serial Number Range 102394262 - 102974610; Model # 1909794 - 102884276; Model # 1909796 - 102440024 -…Model # 190973 - Serial Number Range 102394262 - 102974610; Model # 1909794 - 102884276; Model # 1909796 - 102440024 - 102981676; Model # 1909797 - 102757564 - 102958935; Model # 1909798 - 102831498 - 102831519; Model # 1909799 - 102393683 - 102969656

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-0391-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.