Medical DeviceMar 11, 2015
Zipline Medical Zip 8i Surgical Skin Closure Device recall — FDA Z-1234-2015
The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.
Class IIFDA: TerminatedZipline Medical
Recall history in this database
Classification mix: Class II: 3.
Medical DeviceMar 11, 2015
Zipline Medical Zip 8M Wound Closure Device recall — FDA Z-1235-2015
The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.
Class IIFDA: TerminatedZipline Medical
Medical DeviceMar 11, 2015
Zipline Medical Zip 16 Surgical Skin Closure Device recall — FDA Z-1236-2015
The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.
Class IIFDA: TerminatedZipline Medical
Understanding this recall history
This page summarizes recall records in which the official source identifies Zipline Medical 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.