FDA Device Intelligence
Home › AMERICAN BIO MEDICA CORPORATION › Rapid ONE

Rapid ONE

AMERICAN BIO MEDICA CORPORATION · Model 10-COCS-000 · UDI-DI 10694644800040

LCMLFGLDJJXNDJGDJRDJCDIOJXMDISDKG Prescription
10
510(k) clearances
5
Adverse events
1
Recalls
94
Facilities

Description

Cocaine pouched strips 100/box

Recalls

DateFirmReason
2005-05-31Applied Biotech IncThe firm has discovered that a number of distributed devices of the Medplus ER Drug Screen Test may be incorrectly assembled which may give incorrect results. The product is an in

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.