Multifire VersaTrack Auto Suture Hernia Stapler — Class II medical device recall Z-2252-2020
Ongoing recall by Covidien Llc, reported 2020-06-10. The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly a
| Recall number | Z-2252-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien Llc, Mansfield, MA, United States |
| Recall initiated | 2020-05-12 |
| Classified | 2020-06-03 |
| Reported by FDA | 2020-06-10 |
| Quantity | 12,610 total |
| Lot numbers | P9J0241Y, P9J0242Y, P9J0243Y, P9K1140Y, P9K1141Y, P9K1663Y |
| Model numbers | 174021 |
Product
Multifire VersaTrack Auto Suture Hernia Stapler, 4.0mm, Part No. 174021 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of tissue(s).
Reason for recall
The product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instrument handle is compressed.
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-2252-2020. 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.