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

Recall Z-0936-2015 — Cervical Extension Machine for Physical Therapy

U.S. FDA — Device Enforcement · United States · 2013-12-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0936-2015
Date of alert
2013-12-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MedX Holdings, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
02511166
Reported risk: Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
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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