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AMY

RANDOX LABORATORIES LIMITED · Model AY7932 · UDI-DI 05055273200652

CIJ Prescription
1
510(k) clearances
1
Adverse events
1
Recalls
6
Facilities

Description

An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, or urine.

Recalls

DateFirmReason
2020-07-10RANDOX LABORATORIES, LTD.Amylase AY3805 batch 480449 and Pancreatic Amylase AY3855 batch 480483 have failed to meet the quoted performance claims prior to expiry on 28th Sept 2020.

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

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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.