FDA Device recall Z-2864-2026
STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
- FDA Device
- Class II
- ongoing
- Published 2026-08-12
On 2026-08-12 the FDA classified a Class II recall of STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640 by Stryker, citing there has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2864-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-08 |
| Published | 2026-08-12 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Stryker |
| Distribution | US |
Product
STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
Reason
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Identifiers
| code_info | GTIN 07613327061475, Batch Number: 24284FG2, 24289FG2, 24313FG2, 24322FG2, 24338FG2, 24344FG2, 24351FG2, 25009FG2, 250…GTIN 07613327061475, Batch Number: 24284FG2, 24289FG2, 24313FG2, 24322FG2, 24338FG2, 24344FG2, 24351FG2, 25009FG2, 25036FG2, 25062FG2, 25091FG2, 25129FG2, 25161FG2. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2864-2026%22
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