FDA recall record

GVS TM SQ40S Blood Transfusion Filter recall — FDA Z-1157-2026

Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be…

Class IIclassification
Z-1157-2026official record ID
Jan 28, 2026report date

Recall record at a glance

Official recordZ-1157-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGVS TM, Inc.
Report dateJan 28, 2026
Recall initiation dateNov 3, 2025
Quantity2,720 filters
LocationCovina, CA, United States

Official product description

SQ40S Blood Transfusion Filter

Why the product was recalled

Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.

Distribution information

U.S.: ID, NV, SC, MO, TX, CO, MD, CA, VA, DC, PA, IL, OH, AZ, FL, OK, MN, KY, OR, NE, NC, LA, MS, MI, NY, GA, AL, MA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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