Z-Medica, LLC: Medical Device Recall in 2018 - (Recall #: Z-0925-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

QuikClot TraumaPad, Part# 460 a topical dressing for local management of bleeding wounds such as cuts, lacerations, and abrasions. It may also be used for temporary treatment of severely bleeding wounds such as surgical wounds (operative, postoperative, dermatological, etc.) and traumatic injuries

Product Classification:

Class II

Date Initiated: November 17, 2017

Date Posted: March 14, 2018

Recall Number: Z-0925-2018

Event ID: 79407

Reason for Recall:

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 identified as QuikClot Trauma Pad. The customer alleged that when the pouch was opened, it contained a QuikClot TraumaPad. All 10 pouches in the box had the correct part number, lot number, and expiration date for the prod uct (QuikClot TraumaPad).

Status: Terminated

Product Quantity: 4890

Code Information:

Part# 460, Lot# 7397

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated