Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code:… — Class II medical device recall Z-2622-2017
Terminated recall by Covidien LLC, reported 2017-07-05, distributed nationwide. Cotton tip of the device may disengage due to insufficient adhesive
| Recall number | Z-2622-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, North Haven, CT, United States |
| Recall initiated | 2017-05-09 |
| Classified | 2017-06-23 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2019-02-13 |
| Distributed | Nationwide (US) |
| Quantity | 194,851 |
| Lot numbers | 2020-OCTOBER, M5K04X, M7A01X |
| Model numbers | 173019 |
Product
Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: 173019 The instrument has indications in endoscopic surgery for swabbing small amounts of fluid or for blunt dissection of soft tissue(s) and structures, or as an aid in controlling minor intraoperative bleeding
Reason for recall
Cotton tip of the device may disengage due to insufficient adhesive
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-2622-2017. 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.