Data Foundry

Medical device recalls 2025

3gAllergy Specific IgE Universal Kit — Class II medical device recall Z-0492-2026

Ongoing recall by Siemens Healthcare Diagnostics, Inc., reported 2025-11-19, distributed nationwide. The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holde

Recall numberZ-0492-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSiemens Healthcare Diagnostics, Inc., East Walpole, MA, United States
Recall initiated2025-10-06
Classified2025-11-13
Reported by FDA2025-11-19
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BE, BR, CL, CO, CR, CZ, DE, EE, ES, FR, GB, GR, GT, HK, HR, HU, IL, IT, LV, MX, NL, NO, PA, PK, PL, PT, RO, RS, SE, SK, TR, UA, UY
Quantity2,802 units
Reason classesundeclared allergen
UPC / GTIN / UDI-DI00630414962269
Lot numbers169, 170, 171, 172
Model numbersL2KUN6

Product

3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UNS1), 3gAllergy Specific IgE Control Antibody (L2UNS2); Siemens Material Number (SMN): 10380875; Catalog Number: L2KUN6;

Reason for recall

The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0492-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.