FDA Device recall Z-2464-2015
Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE
- FDA Device
- Class II
- terminated
- Published 2015-09-02
On 2015-09-02 the FDA classified a Class II recall of Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE by Trilliant Surgical, citing sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Systems were reported to occasionally be difficult to remove from the sterilization tray.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2464-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-20 |
| Published | 2015-09-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Trilliant Surgical |
| Distribution | US |
Product
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 Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis and osteotomies of the small bones in the hand and foot. The implants and guide wires are intended for single use only.
Reason
Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Systems were reported to occasionally be difficult to remove from the sterilization tray.
Identifiers
| code_info | Lot Numbers ALU120514552473 and 45479 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2464-2015%22
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