# FDA recall Z-2622-2017

> **Covidien LLC** · Class II · device recall initiated 2017-05-09.

## 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

## Distribution

Nationwide Distribution

## Key facts

- **Recall number:** Z-2622-2017
- **Recalling firm:** Covidien LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-09
- **Report date:** 2017-07-05
- **Termination date:** 2019-02-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** North Haven, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2622-2017

## Citation

> AI Analytics. FDA recall Z-2622-2017. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2622-2017. Source: US FDA. Licensed CC0.

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