PlainRecalls
FDA Devices Moderate Class II Terminated

QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200

Reported: November 17, 2021 Initiated: September 22, 2021 #Z-0211-2022

Product Description

QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200

Reason for Recall

Lack of Packaging seal integrity may result in a sterile barrier breach.

Details

Recalling Firm
Z-Medica, LLC
Units Affected
2400 units
Distribution
US Nationwide distribution in the state of NC.
Location
Wallingford, CT

Frequently Asked Questions

What product was recalled?
QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200. Recalled by Z-Medica, LLC. Units affected: 2400 units.
Why was this product recalled?
Lack of Packaging seal integrity may result in a sterile barrier breach.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 17, 2021. Severity: Moderate. Recall number: Z-0211-2022.