Horizon 24 Large Titanium Clips with Adhesive Backing — Class II medical device recall Z-2327-2016
Terminated recall by Teleflex Medical, reported 2016-08-10, distributed in AL, AZ, CA, CT, FL, IL, KY, MD…. The manufacturing and expiration dates are not printed on the blister pack label.
| Recall number | Z-2327-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Morrisville, NC, United States |
| Recall initiated | 2013-08-08 |
| Classified | 2016-08-03 |
| Reported by FDA | 2016-08-10 |
| Terminated | 2016-08-15 |
| Distributed | AL, AZ, CA, CT, FL, IL, KY, MD, MI, MN, NC, NM, NY, OR, PA, SC, TX, VA, WA, WI |
| Countries outside the US | CA |
| Quantity | 8,220 units |
| Reason classes | labeling |
| Serial numbers | 01J1200435 |
| Model numbers | 004204 |
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 for recall
The manufacturing and expiration dates are not printed on the blister pack label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2327-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.