Origen Biomedical, Inc.
7000 Burleson Rd. Bldg D, Austin, TX, US
Registered product codes
6 product codes
Recent MDR events
35 on file
- SPIKE ADAPTERAug 8, 2025MalfunctionMW5174282
- SPIKE ADAPTER - TWO SPIKES TO ONE SPIKE PORT WITH 20CM SCD TUBING AND PINCH CLAMJun 17, 2025InjuryMW5171579
- PERMALIFE CELL CULTURE BAGDec 6, 2024Malfunction1000160256-2024-00008
- CS550S CRYOSTORE FREEZINGBAGOct 8, 2024Injury1000160256-2024-00007
- SPIKE COUPLERMar 15, 2024Malfunction18911824
- CRYOSTOREFeb 14, 2024Malfunction1000160256-2024-00002
- CRYOSTORE CS500NSep 30, 2021MalfunctionMW5104308
- ORIGEN EVOLVE 3000 ML CRYOPRESERVATION BAGOct 16, 2020InjuryMW5097317
- ORIGEN REINFORCED DUAL LUMEN CATHETERJan 10, 2020Malfunction1646848-2020-00001
- ORIGEN REINFORCED DUAL LUMEN CATHETERApr 2, 2019Malfunction1646848-2019-00014
Recalls
20 on file
- Open, ClassifiedFeb 9, 2024
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.
View FDA record ↗ - TerminatedApr 10, 2021
It was identified that tissue culture bags were incorrectly labeled as free of phthalates.
View FDA record ↗ - TerminatedJun 4, 2019
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
View FDA record ↗ - TerminatedJun 4, 2019
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
View FDA record ↗ - TerminatedJun 4, 2019
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
View FDA record ↗ - TerminatedJun 4, 2019
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
View FDA record ↗ - TerminatedJun 4, 2019
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
View FDA record ↗ - TerminatedJun 4, 2019
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
View FDA record ↗ - TerminatedNov 7, 2018
Potential for clear extension tube to separate from the hub, which could result in blood loss and may require intervention to prevent permanent impairment/damage
View FDA record ↗ - TerminatedOct 20, 2017
Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen ECMO Catheter has had a separation of the clear extension tube from the hub connection. These adverse events resulted in patient injury (blood loss).
View FDA record ↗
Compliance history
Matched by FEI 1000160256.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.