FDA Device Intelligence
Home › MAST GROUP LIMITED › Mast Assure

Mast Assure

MAST GROUP LIMITED · Model M10308 · UDI-DI 15060392376154

GRM Prescription
10
510(k) clearances
14
Adverse events
1
Recalls
14
Facilities

Description

POLY O Factor O2, O4, O7, O8, O9, O9, 46, O3, 10 and O1,3,19

Recalls

DateFirmReason
2026-03-25Remel Europe Ltd.Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O seroty

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.