FDA Device recall Z-1841-2017
Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX TRUNAV Retrograde Drill is intended for use in creati…
- FDA Device
- Class II
- terminated
- Published 2017-04-26
On 2017-04-26 the FDA classified a Class II recall of Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX TRUNAV Retrograde Drill is intended for use in creati… by Smith And Nephew, citing potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1841-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-15 |
| Published | 2017-04-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Smith And Nephew |
| Distribution | US |
Product
Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
Reason
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
Identifiers
| code_info | Batch Numbers: F93290, F93297, G10709, G10712, G15944, G15945, G27849 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1841-2017%22
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