Z-Medica recalls QuikClot TraumaPad Part# 460 due to one pouch in a box containing the wrong type. All other pouches and packaging are correct. No action needed as the hazard is a labeling error, not a safety risk.
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).
Z-Medica is recalling some boxes of QuikClot TraumaPad Part# 460 because one pouch in a box of 10 was labeled incorrectly as QuikClot Roll instead of QuikClot TraumaPad. This is a labeling error, not a safety hazard, so no action is required.
The hazard is a labeling error where one pouch in a box of 10 was incorrectly labeled as QuikClot Roll instead of QuikClot TraumaPad. However, the customer reported that the pouch contained the correct QuikClot TraumaPad product when opened, so there is no safety risk.
Anyone who owns or uses QuikClot TraumaPad Part# 460. The risk is minimal as the error only affects one pouch per box and the rest of the product is correctly labeled.
Check if your box of QuikClot TraumaPad Part# 460 contains one pouch labeled "QuikClot Roll" instead of "QuikClot TraumaPad". All other pouches and packaging are correctly labeled.
Inspect each pouch in your box to ensure it is labeled "QuikClot TraumaPad". If one pouch is labeled "QuikClot Roll", it is part of the recalled batch.
No, this is a labeling error. The customer reported that the pouch contained the correct QuikClot TraumaPad product when opened, so there is no safety risk.
No action is needed. The recall is for labeling, not a safety issue, so you can continue using the product as normal.
Check if your box of QuikClot TraumaPad Part# 460 contains one pouch labeled "QuikClot Roll" instead of "QuikClot TraumaPad".
We’ve drafted a message you can send Z-Medica to request your refund or repair — edit it as you like.
Subject: Recall Z-0925-2018 — Z-Medica Z-Medica Hello, I own a Z-Medica that is covered by recall Z-0925-2018 from Z-Medica. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
