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

Recall Z-1718-2015 — Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction)

U.S. FDA — Device Enforcement · United States · 2015-05-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1718-2015
Date of alert
2015-05-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Advanced Back Technologies, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07071003
Reported risk: Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs
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.

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