Covidien LLC: Medical Device Recall in 2017 - (Recall #: Z-2622-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 9, 2017

Date Posted: July 5, 2017

Recall Number: Z-2622-2017

Event ID: 77300

Reason for Recall:

Cotton tip of the device may disengage due to insufficient adhesive

Status: Terminated

Product Quantity: 194,851

Code Information:

Lot Numbers: M5K04X to M7A01X Exp Date: 2020-October through 2022-January

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated