Fresh Recalls

FDAClass II · Medical device · Recall Z-2936-2026 · Recalled August 19, 2026

BIOFIRE Respiratory Panel 2 recall — BioFire Diagnostics, LLC

Agency report date: August 19, 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 Respiratory Panel 2
Company / brand
BioFire Diagnostics
Lot / serial / date codes
Part Number: 423742 UDI-DI code: 00815381020529 Pouch Lot: 3VLB25 Kit Lot: 1872125
Distribution
U.S. Nationwide distribution in the states of AL, AR, IA, IL, KS, LA, MN, MO, TX, and WI.
Agency product description and boundaries

BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic

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: Due to increase in false negative results

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 Respiratory Panel 2

3. Open the official notice or contact

Official recall ID
Z-2936-2026
Brand
BioFire Diagnostics
Classification
Class II
Units affected
2,370 pouches (79 kits)
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
Part Number: 423742 UDI-DI code: 00815381020529 Pouch Lot: 3VLB25 Kit Lot: 1872125
Distribution
U.S. Nationwide distribution in the states of AL, AR, IA, IL, KS, LA, MN, MO, TX, and WI.
FDA event ID
99261
Recall initiated
June 24, 2026
FDA classified
August 12, 2026
FDA report date
August 19, 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 September 7, 2026 at 6:00 AM UTC.

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