Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound recall — FDA Z-0179-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Recall history in this database
Classification mix: Class II: 6.
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound recall — FDA Z-0181-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound recall — FDA Z-0183-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound recall — FDA Z-0180-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex Med 4" - Product Usage: Single Use secondary wound recall — FDA Z-0184-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Medical DeviceOct 30, 2019
Andover Healthcare Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound recall — FDA Z-0182-2020
Incomplete packaging seal of sterile product
Class IIFDA: TerminatedAndover Healthcare Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Andover Healthcare Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.