Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351
FDA Recall Z-0693-2020 · Posted None
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Recalling FirmMedtronic Perfusion Systems
Recall StatusTerminated
Product CodeDTM
Date Initiated2019-11-14
Date Terminated2020-10-05
Product Quantity24 units
Reason for Recall
Medtronic has identified an out of-specification condition exhibiting excess plastic (flash) in the arterial filter directly above the outlet port.
Firm Action
Beginning 14-Nov-2019, Medtronic initiated an immediate Urgent Medical Device Recall via verbal communication to one (1) customer that was shipped the affected product according to Medtronic records. The customer was asked to identify and quarantine any unused affected product.
The immediate communication was followed by a written urgent medical device recall notification beginning on 26-Nov-2019 to communicate the issue to the one (1) customer that received affected product. The consignee was asked to confirm receipt of urgent medical device recall notification via a Customer Confirmation Certificate. Medtronic is seeking the return of the affected product.
Root Cause
Process control
Distribution Pattern
CA
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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