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

Recall Z-1185-2016 — Transport Stretcher, and Head and Neck Surgery Stretcher Non-powered stretcher

U.S. FDA — Device Enforcement · United States · 2016-02-05 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1185-2016
Date of alert
2016-02-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Medical Division of Stryker Corporation
Product category
device
Product type
Devices
Reported risk: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactured using the incorrect oil. The oil used does not contain the same wear resistance additives as the specified oils and therefore its use increases the potential for wear which may cause a leak event or jack drift. Testing was done to evaluate the jacks with incorrect oil and leak events we
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.

Related

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.