Lower riskMedical device recall · FDA · Published November 17, 2017
Z-Medica QuikClot TraumaPad Recall: Wrong Pouch Type in Some Boxes
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 QuikClot TraumaPad Recall: Wrong Pouch Type in Some Boxes.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/72524-z-medica-quikclot-traumapad-recall-wrong-pouch-type-in-some. Based on FDA recall #Z-0925-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0925-2018%22&limit=1).
Z-Medica, LLC recalled QuikClot TraumaPad, Part# 460, after a customer reported receiving a QuikClot Roll pouch instead of the correct TraumaPad pouch. The Food and Drug Administration announced the Class II recall on November 17, 2017.
How to tell if you have it
Brand: Z-Medica
Product: QuikClot TraumaPad
Part#: 460
Lot#: 7397
The hazard
A customer complained that one of the pouches in a box of 10 had "QuikClot Roll" instead of "QuikClot TraumaPad." 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 product.
Context
GovInfoNow's records show Z-Medica, LLC has 1 other recall on record since 2021-09-22. On 2021-09-22, Z-Medica issued a QuikClot Combat Gauze Recall due to sterile barrier risk from lack of packaging seal integrity. Other recent recalls of similar products include Medline TRACH TUBE Kit Recall (2026-07-10), Medline EYE TRAY-LF Kit Recall (2026-04-10), and Microbiologics KWIK-STIK Quality Control Kit Recall (2025-11-13).
How to tell if you have this one
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.
Brand
Z-Medica
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Pouch Labels
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.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationally” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0925-2018 (November 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0925-2018 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.