Fresh Recalls

FDAClass II · Medical device · Recall Z-2746-2026 · Recalled July 22, 2026

ST AIA-Pack Testosterone recall — Tosoh Bioscience Inc

Agency report date: July 22, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
ST AIA-Pack Testosterone
Company / brand
Tosoh Bioscience
Lot / serial / date codes
UDI-DI: 14560189210032; Lot Numbers: FX12404, FY12407, FY12406, FZ12408
Distribution
Global Distribution. US Nationwide.
Agency product description and boundaries

ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause falsely elevated or falsely low total testosterone results. Such erroneous test results may lead to additional testing/diagnostic interventions and in limited cases, may lead to a delay in diagnosis and/or initiation of unnecessary or incorrect clinical treatment measures.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: ST AIA-Pack Testosterone recall status

3. Open the official notice or contact

Official recall ID
Z-2746-2026
Brand
All Tosoh Bioscience recalls
Classification
Class II
Units affected
310 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Grove City, OH, United States
Firm address
3600 Gantz Rd, 43123-1895

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI: 14560189210032; Lot Numbers: FX12404, FY12407, FY12406, FZ12408
Distribution
Global Distribution. US Nationwide.
Firm notified the public via
Letter
FDA event ID
99210
Recall initiated
June 12, 2026
FDA classified
July 16, 2026
FDA report date
July 22, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 20, 2026 at 6:00 PM UTC.

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