OXY-1 System, Model Number 001-0500-001. Used during cardiopulmonary bypass. OXY-1 System consists of Console, Pump Drive, E Drive, and Pole Mount. The disposable Pump Lung Unit PLU part number 001-0400-100 is sold separately and is not part of this recall.
FDA Recall Z-0550-2022 · Posted 2022-02-03
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Recalling FirmAbiomed, Inc.
Recall StatusTerminated
Product CodeDTZ
Date Initiated2021-12-14
Date Terminated2023-02-28
Product Quantity42 Units
Reason for Recall
The firm has received complaints of the OXY-1 System Console experiencing a power interruption while in use, which disrupts therapy delivered to a patient on support. Disruption of therapy could lead to prolonged hypoxia.
Firm Action
The firm began notifying customers by phone starting December 14, 2021. The firm followed up by sending Urgent Medical Device Recall letters to customers on January 20, 2022.
The firm is requesting that customers return their devices. The firm does not recommend placing new patients on support. For patients currently on support with an affected system, the firm recommends physicians use their clinical judgement on whether it is appropriate to continue a patient on the OXY-1 System or to transition that patient to the next step in their clinical journey.
The letter included instructions on how to return impacted product. If you have questions on returning product, If you have any
questions, please contact Diane Welsh from Abiomed s customer service team at (978) 646-1467 or email [email protected]. The firm's Clinical field staff will be available to coordinate boxing and shipping of the OXY-1 system for return to Abiomed.
If you have questions regarding this recall, please contact Ralph Barisano directly at
(978) 882-8068.
Root Cause
Software design (manufacturing process)
Distribution Pattern
US distribution to FL, GA, IN, MD, NC, PA, TX.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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