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

Recall Z-2464-2015 — Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE; Combined Tiger/Headless Screw Part # 210-99-101 NON-STERILE; These are components of the Tiger Cannulated Screw System and the Tiger Headless Cannulated Screw System The Tiger Cannulated Screw Fixation System and the Tiger Headless Cannulat

U.S. FDA — Device Enforcement · United States · 2015-07-20 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2464-2015
Date of alert: 2015-07-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Trilliant Surgical Ltd.
Product category: device
Product type: Devices

Reported risk: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Systems were reported to occasionally be difficult to remove from the sterilization tray.

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.

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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