Zipline Medical: Medical Device Recall in 2015 - (Recall #: Z-1235-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Zip 8M Wound Closure Device; for wounds up to 8 cm in length; Product number PS9080; Rx only, Sterile Indicated for use during and after skin incision procedures to approximate skin and hold together skin edges until healing can take place.

Product Classification:

Class II

Date Initiated: February 5, 2015

Date Posted: March 11, 2015

Recall Number: Z-1235-2015

Event ID: 70466

Reason for Recall:

The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.

Status: Terminated

Product Quantity: 3109 devices, total all model numbers

Code Information:

Lot 1002750, Exp 2016-09

Distribution Pattern:

Worldwide Distribution - US Nationwide and the countries of Panama, Tehran, Ireland, Sweden, Japan, Hong Kong, Finland, Pakistan, Taiwan, Malaysia.

Voluntary or Mandated:

Voluntary: Firm initiated