FDA Device recall Z-1468-2022
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
- FDA Device
- Class II
- ongoing
- Published 2022-08-03
On 2022-08-03 the FDA classified a Class II recall of HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile) by Paragon 28, citing due to Titanium plasma coating not present implant.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1468-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-05-26 |
| Published | 2022-08-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Paragon 28 |
| Distribution | US |
Product
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Reason
Due to Titanium plasma coating not present implant.
Identifiers
| code_info | Part Number: P40-002-0275-S UDI-DI Code: (01)00889795033987(17)270323(10)26010822202 Lot Number: 26010822202 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
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FDA Device · Class II · 2026-07-29 · Paragon 28 - Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S
FDA Device · Class II · 2025-12-10 · Paragon 28 - Phantom TTC Nail, 10.0 X 200mm, Right
FDA Device · Class II · 2024-03-13 · Paragon 28
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1468-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.