Fresh Recalls

FDAClass II · Medical device · Recall Z-2081-2026 · Recalled May 13, 2026

Biofire Spotfire Respiratory/Sore Throat Panel REF recall — BioFire Diagnostics, LLC

Agency report date: May 13, 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
Biofire Spotfire Respiratory/Sore Throat Panel REF
Company / brand
BioFire Diagnostics
Lot / serial / date codes
Lot Number: 2215125/UDI: 00815381020390
Distribution
US Nationwide distribution in the states of MS, TX MN, VA.
Agency product description and boundaries

Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485

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: Respiratory/sore throat panel test may result in false negative results and control failures.

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: Biofire Spotfire Respiratory/Sore Throat Panel REF

3. Open the official notice or contact

Official recall ID
Z-2081-2026
Brand
BioFire Diagnostics
Classification
Class II
Units affected
2400 pouches
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Salt Lake City, UT, United States
Firm address
515 S Colorow Dr, 84108-1248

Identifying details (verbatim from the notice)

Product codes / lots
Lot Number: 2215125/UDI: 00815381020390
Distribution
US Nationwide distribution in the states of MS, TX MN, VA.
Firm notified the public via
E-Mail
FDA event ID
98719
Recall initiated
April 1, 2026
FDA classified
May 6, 2026
FDA report date
May 13, 2026
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 September 7, 2026 at 6:00 AM UTC. Record retrieved August 11, 2026 at 6:00 PM UTC.

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