OriGen Biomedical, Inc. 3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only
Brand
OriGen Biomedical, Inc.
Lot Codes / Batch Numbers
Lot # 042417-5045
Products Sold
Lot # 042417-5045
OriGen Biomedical, Inc. is recalling 3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only due to The firm has become aware that they have distributed product that was expired.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm has become aware that they have distributed product that was expired.
Recommended Action
Per FDA guidance
On 6/24/2019, a email was sent to the affected customer informing them that the product was expired and requesting that it be returned.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
TX
Page updated: Jan 10, 2026