Home/Recalls/FDA-Z-1559-2026
FDA DevicesClass II

Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolyti...

Published: March 18, 2026Recall ID: Z-1559-2026Category: devicesCountry: US

Reason for Recall / Hazard

Product not cleared by the FDA.

Product Description & Identification

Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection.

Additional Source Details

FieldValue
CityMassing
StateN/A
Event id98472
Address 1Morolding 6
Address 2N/A
Code infoModel No. 41972; No UDI; Lot Code: 6933289812337.
Postal codeN/A
Report date20260318
Product typeDevices
Product quantity188 units
Reason for recallProduct not cleared by the FDA.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251219
Initial firm notificationOther
Center classification date20260312

Overview

  • Recalling FirmAltruan GmbH
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution.
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