Reported Aug 19, 2026 · Terminated · Updated Sep 16, 2026
Pooled Cryoprecipitated AHF
Blood Assurance Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Blood Assurance Inc · 705 E 4th St · Chattanooga, TN · 37403-1916
Is this the product you have?
- Pooled Cryoprecipitated AHF
- Lot codes and dates
- W043225118379
- Amount recalled
- 1
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Pooled Cryoprecipitated AHF, collected from a donor who had received a dura mater graft and was at increased risk for Creutzfeldt-Jakob Disease (CJD), were distributed.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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