FDA Device recall Z-2327-2016
Horizon 24 Large Titanium Clips with Adhesive Backing, Ref 004204, Rx Only, Sterile
- FDA Device
- Class II
- terminated
- Published 2016-08-10
On 2016-08-10 the FDA classified a Class II recall of Horizon 24 Large Titanium Clips with Adhesive Backing, Ref 004204, Rx Only, Sterile by Teleflex Medical, citing the manufacturing and expiration dates are not printed on the blister pack label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2327-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-08-08 |
| Published | 2016-08-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | AL, AZ, CA, CT, FL, IL, KY, MD, MI, MN, NC, NM, NY, OR, PA, SC, TX, VA, WA, WI |
Product
Horizon 24 Large Titanium Clips with Adhesive Backing, Ref 004204, Rx Only, Sterile. The metal ligating clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice. An implantable clip is a clip-like device intended to connect internal tissues to aid healing. It is not absorbable
Reason
The manufacturing and expiration dates are not printed on the blister pack label.
Identifiers
| code_info | Lot/Serial Number 01J1200435 |
|---|
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-2327-2016%22
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