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

Recall Z-0645-2019 — IMRIS T2X table, Part Numbers: (a)108000-000, (b)108000-600, (c)109682-000, (d) 109682-600, (e) 110470-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indi

U.S. FDA — Device Enforcement · United States · 2018-11-06 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0645-2019
Date of alert: 2018-11-06
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Deerfield Imaging, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10000983

Reported risk: Table may drift in the roll position while in use

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

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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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