OriGen Biomedical, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0318-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only

Product Classification:

Class II

Date Initiated: June 24, 2019

Date Posted: November 11, 2020

Recall Number: Z-0318-2021

Event ID: 85124

Reason for Recall:

The firm has become aware that they have distributed product that was expired.

Status: Terminated

Product Quantity: 6 units

Code Information:

Lot # 042417-5045

Distribution Pattern:

US: TX

Voluntary or Mandated:

Voluntary: Firm initiated