FDA Device recall Z-0765-2017
Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry f…
- FDA Device
- Class II
- terminated
- Published 2016-12-21
On 2016-12-21 the FDA classified a Class II recall of Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry f… by Stryker Sustainability Solutions, citing an increase in reports indicating that the reprocessed H12LP Trocar adjustable plug may break in the packaging or during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0765-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-11 |
| Published | 2016-12-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | US |
Product
Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry for endoscopic instruments in patients requiring minimally invasive surgical procedures.
Reason
An increase in reports indicating that the reprocessed H12LP Trocar adjustable plug may break in the packaging or during use.
Identifiers
| code_info | Model Lot Manufacture Date Expiration H12LP 3 5 3 6 585 3/3/2015 Mar-18 H12LP 3 5 3 6 880 3/3/2015 Mar-18 H12LP 3 5…Model Lot Manufacture Date Expiration H12LP 3 5 3 6 585 3/3/2015 Mar-18 H12LP 3 5 3 6 880 3/3/2015 Mar-18 H12LP 3 5 3 9 579 3/3/2015 Mar-18 H12LP 3 5 4 0 175 3/5/2015 Mar-18 H12LP 3 5 4 2 016 3/5/2015 Mar-18 H12LP 3 5 4 3 606 3/5/2015 Mar-18 H12LP 3 5 4 3 610 3/9/2015 Mar-18 H12LP 3 5 4 6 115 3/9/2015 Mar-18 H12LP 3 5 4 6 751 3/9/2015 Mar-18 H12LP 3 5 4 6 767 3/9/2015 Mar-18 H12LP 3 5 4 8 518 3/11/2015 Mar-18 H12LP 3 5 4 8 368 3/13/2015 Mar-18 H12LP 3 5 4 9 294 3/13/2015 Mar-18 H12LP 3 5 4 9 583 3/13/2015 Mar-18 H12LP 3 5 5 7 373 3/16/2015 Mar-18 H12LP 3 5 5 9 424 3/16/2015 Mar-18 H12LP 3 5 5 9 453 3/16/2015 Mar-18 H12LP 3 5 6 0 044 3/16/2015 Mar-18 H12LP 3 5 6 0 160 3/16/2015 Mar-18 H12LP 3 5 6 1 254 3/16/2015 Mar-18 H12LP 3 5 6 1 368 3/16/2015 Mar-18 H12LP 3 5 6 1 797 3/16/2015 Mar-18 H12LP 3 5 6 2 147 3/16/2015 Mar-18 H12LP 3 5 6 2 759 3/16/2015 Mar-18 H12LP 3 5 6 2 771 3/16/2015 Mar-18 H12LP 3 5 6 4 013 3/16/2015 Mar-18 H12LP 3 5 6 7 588 3/20/2015 Mar-18 |
|---|
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-0765-2017%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.