Fresh Recalls

FDAClass II · Medical device · Recall Z-2171-2026 · Recalled May 20, 2026

ZYMUTEST HIA IgG recall — Aniara Diagnostica LLC

Agency report date: May 20, 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
ZYMUTEST HIA IgG
Company / brand
Aniara Diagnostica
Lot / serial / date codes
UDI-DI: 03663537018763; Lot Number: FD1265
Distribution
US Nationwide distribution in the states of CA, GA, MN, MO, NC, NM, NY, VA, WA, and WI
Agency product description and boundaries

ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A

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FDA reports: Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.

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: ZYMUTEST HIA IgG

3. Open the official notice or contact

Official recall ID
Z-2171-2026
Brand
Aniara Diagnostica
Classification
Class II
Units affected
359 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
West Chester, OH, United States
Firm address
7768 Service Center Dr, 45069-2442

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI: 03663537018763; Lot Number: FD1265
Distribution
US Nationwide distribution in the states of CA, GA, MN, MO, NC, NM, NY, VA, WA, and WI
Firm notified the public via
Letter
FDA event ID
98754
Recall initiated
April 1, 2026
FDA classified
May 12, 2026
FDA report date
May 20, 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 18, 2026 at 6:00 PM UTC.

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