Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0805-2025 — The FastPack IP Sex Hormone Binding Globulin Immunoassay, Part #25000081, is for the quantitative measurement of SHBG in human serum and plasma. For in vitro diagnostic Use and contains 30 FastPacks.

U.S. FDA — Device Enforcement · United States · 2024-12-03 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0805-2025
Date of alert
2024-12-03
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Qualigen Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20816467020345
Reported risk: Three lots of the FastPacks kitted into the FastPack SHBG Complete Kits were labeled with the incorrect expiration date. The following is a listing of affected lots: Lot Number: 2408018-1, 2409015-1, and 2409015-2. The likelihood of patient harm is expected to be low as routine Quality Control should detect kits that are impacted by signal deterioration due to age.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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