Instrumentation Laboratory 2025-12-24 Health moderate FDA
Health · FDA · Recall #FDA-Z-0938-2026
HemosIL SynthAFax. Partial Thromboplastin Time Tests. Recall
Issued December 24, 2025 · Instrumentation Laboratory
In December 2025, Instrumentation Laboratory recalled the HemosIL SynthAFax. Partial Thromboplastin Time Tests., a moderate health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Recalled lots were manufactured with double the amount of preservative concentration.
What you should do
- 1 Stop using HemosIL SynthAFax. Partial Thromboplastin Time Tests. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Instrumentation Laboratory to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Instrumentation Laboratory
- Category
- Health
- Recall date
- December 24, 2025
- Units affected
- Not reported
- Sold at
- Domestic: CA, CO, FL, NY; Foreign: AR, AT, CA, CZ, DE, DK, ES, FR, GB, IE, IL, IN, IT, JP, LK, NL, PL, PT, RO, RS, TH, VN.
- Recall number
- FDA-Z-0938-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Instrumentation Laboratory has 6 recalls in our database.
- We're tracking 3,707 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.