Andover Healthcare Inc.: Medical Device Recall in 2019 - (Recall #: Z-0181-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap

Product Classification:

Class II

Date Initiated: June 19, 2019

Date Posted: October 30, 2019

Recall Number: Z-0181-2020

Event ID: 83239

Reason for Recall:

Incomplete packaging seal of sterile product

Status: Terminated

Product Quantity: 330 Cases

Code Information:

Manufacturer's product or Catalog # 9300S Expiration Date: 01OCT2021-14JUN2022 LOT # CIOZJV, CI02SW, CI18YA, CI1FJ2

Distribution Pattern:

US Nationwide distribution including the states of MA, TX, RI, OH, NY, MN, SD, IL, MO, FL, VA, NE, UT, CA

Voluntary or Mandated:

Voluntary: Firm initiated