FDA Device recall Z-2733-2020
Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone sc…
- FDA Device
- Class II
- terminated
- Published 2020-08-05
On 2020-08-05 the FDA classified a Class II recall of Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone sc… by Arthrex, citing screws provided in packaging are 5mm shorter than intended.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2733-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-24 |
| Published | 2020-08-05 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Arthrex |
| Distribution | n/a |
Product
Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions.
Reason
Screws provided in packaging are 5mm shorter than intended
Identifiers
| code_info | Batch Number: 10706233 UDI Number:00888867056411 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2733-2020%22
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