Official recall notice

FDA DeviceClass IINotable

FDA Recall: Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp ver

Recall date
2026-08-12
FDA class
Class II

Why it was recalled

Hazard

Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.

Product description

Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.

Affected products

Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2

Verify with the official notice →
Share:

Related Recalls

2026-09-23 · FDA_DEVICE
FDA Recall: Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
AVID Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from
Howmedica Osteonics Corp.
2026-09-23 · FDA_DEVICE
FDA Recall: Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number:
Medline Industries, LP
2026-09-23 · FDA_DEVICE
FDA Recall: Happiest Baby, Inc. SNOO Sleep Sack, X-Large Model/Catalog Number: S2101-501 S2101-508-11 S2101-508
Happiest Baby, Inc