# FDA recall Z-0180-2020

> **Andover Healthcare Inc.** · Class II · device recall initiated 2019-06-19.

## 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

- **Recall number:** Z-0180-2020
- **Recalling firm:** Andover Healthcare Inc.
- **Classification:** Class II
- **Product type:** device
- **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

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

## Citation

> AI Analytics. FDA recall Z-0180-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0180-2020. Source: US FDA. Licensed CC0.

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