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RDS
AMERICAN BIO MEDICA CORPORATION · Model 10-10NDS-200 · UDI-DI 10694644300052
JXN
Prescription
1
510(k) clearances
1
Adverse events
2
Recalls
55
Facilities
Description
10 W/8X+MTD,PPX opi 20 BULKPAC
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-10-04 | Express Diagnostics Int'l., Inc. | Express Diagnostics Int'l, Inc (EDI), is recalling DrugCheck Drug Screen Cups containing buprenorphine (BUP) and propoxyphene (PPX) because they must be labeled as "forensic use o |
| 2008-05-28 | Sun Biomedical Laboratories, Inc. | Product was sold while the devices were under FDA 510 (k) review, which was subsequently denied. |
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Get your free API keyRead the docsData 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.