FDA-Device2020-11-11Class II
3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only
OriGen Biomedical, Inc.
Hazard
The firm has become aware that they have distributed product that was expired.
Sold states
US: TX
Affected count
6 units
Manufactured in
7000 Burleson Rd Bldg D, N/A, Austin, TX, United States
Products
3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0318-2021Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief