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Aero-Med

AERO-MED, LLC · Model AMM12325A · UDI-DI 00810010895004

PQD
0
510(k) clearances
19
Adverse events
1
Recalls
53
Facilities

Description

Peak Test DBS Specimen Collect and Trans Kit (Single Card)

Recalls

DateFirmReason
2022-03-16LetsGetChecked Inc.Users received sample collection kits that were assigned to another user. Incorrect shipping labels were applied to the collection kits. As a result, a number of users received sa

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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.