FDA recall Z-0180-2020

Product

Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap

Reason for recall

Incomplete packaging seal of sterile product

Distribution

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

Key facts

Status

Terminated

Initiation date

2019-06-19

Report date

2019-10-30

Termination date

2020-09-09

Voluntary/Mandated

Voluntary: Firm initiated

Location

Salisbury, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0180-2020