Andover Healthcare, Inc.
Andover Healthcare, Inc. holds FDA 510(k) medical device clearance, cleared in 2009, with 7 FDA device recalls on record.
Top product codes for Andover Healthcare, Inc.
FDA recalls by Andover Healthcare, Inc.
- Z-1828-2024 — Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage, Tan, 4INx5YD (5400S)
- Z-0182-2020 — Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap
- Z-0181-2020 — Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap
- Z-0184-2020 — Sterile Co-Flex Med 4" - Product Usage: Single Use secondary wound dressing or compression wrap
- Z-0179-2020 — Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
- Z-0180-2020 — Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap
- Z-0183-2020 — Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Andover Healthcare, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.