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

Recall Z-0040-2017 — Mobile Column TruSystem 7500, Material Number 1717023; Mobile Column TruSystem 5500, Material Number 1607822 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient tran

U.S. FDA — Device Enforcement · United States · 2016-07-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0040-2017
Date of alert: 2016-07-10
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): 101281354

Reported risk: Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

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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