Medical DeviceNov 17, 2021
Z-Medica QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding recall — FDA Z-0211-2022
Lack of Packaging seal integrity may result in a sterile barrier breach.
Class IIFDA: TerminatedZ-Medica, LLC
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceMar 14, 2018
Z-Medica QuikClot TraumaPad, Part# 460 a topical dressing for local management of bleeding recall — FDA Z-0925-2018
A customer complained that one of the pouches in a box of 10 had "QuikClot Roll" pouch instead of "QuikClot TraumaPad" pouch. The carton as well as the remaining 9 pouches were properly…
Class IIFDA: TerminatedZ-Medica, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies Z-Medica, LLC 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.