Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Reported: October 30, 2019 Initiated: June 19, 2019 #Z-0180-2020
Product Description
Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Reason for Recall
Incomplete packaging seal of sterile product
Details
- Recalling Firm
- Andover Healthcare Inc.
- Units Affected
- 8500 Cases
- Distribution
- US Nationwide distribution including the states of MA, TX, RI, OH, NY, MN, SD, IL, MO, FL, VA, NE, UT, CA
- Location
- Salisbury, MA
Frequently Asked Questions
What product was recalled? ▼
Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap. Recalled by Andover Healthcare Inc.. Units affected: 8500 Cases.
Why was this product recalled? ▼
Incomplete packaging seal of sterile product
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 30, 2019. Severity: Moderate. Recall number: Z-0180-2020.
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