Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0926-2015 — Cable remote control JUX Material, no.1307315, Serial number: to (incl.) 101287649. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating the

U.S. FDA — Device Enforcement · United States · 2014-12-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0926-2015
Date of alert: 2014-12-03
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Trumpf Medical Systems, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 101287649

Reported risk: Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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