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OriGen Biomedical, Inc.

OriGen Biomedical, Inc. Recalls

All product recalls associated with OriGen Biomedical, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Dec 2023

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

Accessory Set Syringes (OriGen) – Qualification Concern (2023)

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 resulted in loss of gamma compatibility, for accessory set syringes that were gamma sterilized, which resulted in yellowed syringes.

FDADec 19, 2023CA, DE, FL +8 more• OriGen Biomedical, Inc.

OriGen Biomedical, Inc.: Evolve Cell Culture Bags, part numbers: EV1000N and EV30...

It was identified that tissue culture bags were incorrectly labeled as free of phthalates.

FDAJan 28, 2021CA, CT, FL +16 more• OriGen Biomedical, Inc.

OriGen Biomedical, Inc.: 3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 08143...

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

FDAJun 24, 2019

• OriGen Biomedical, Inc.