Home › ORIGEN BIOMEDICAL, INC. › Tube Adapter
Tube Adapter
ORIGEN BIOMEDICAL, INC. · Model 15-F-T · UDI-DI 10816203020007
KJG
Prescription
1
510(k) clearances
29
Adverse events
1
Recalls
35
Facilities
Description
One female luer with 15cm of SCD tubing, case of 50
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-19 | OriGen Biomedical, Inc. | Accessory sets contain a syringes not yet qualified for the accessory's intended purpose; due to design changes to the syringe barrels and a polypropylene resin change that resulte |
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 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.
