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

Recall Z-1872-2014 — Shaver Handpiece Sterilization Tray. Model number 272-700-000. For sterilization of Stryker Endoscopy arthroscopic shaver.

U.S. FDA — Device Enforcement · United States · 2014-05-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1872-2014
Date of alert
2014-05-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Endoscopy
Product category
device
Product type
Devices
Reported risk: STERRAD 100S parameters provided in the Shaver Handpiece reprocessing guide (P10299 Revision A) did not fully consider all worst-case scenarios during validation testing.
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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