Data Foundry

Medical device recalls 2014

Medtronic Ascenda Intrathecal Catheter models 8780 and 8781 — Class II medical device recall Z-2172-2014

Terminated recall by Medtronic Neuromodulation, reported 2014-08-20, distributed nationwide. Medtronic is removing specific lots of the Ascenda Intrathecal Catheters and Revision Kits, which are used wit

Recall numberZ-2172-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedtronic Neuromodulation, Minneapolis, MN, United States
Recall initiated2014-07-11
Classified2014-08-08
Reported by FDA2014-08-20
Terminated2015-07-17
DistributedNationwide (US)
Countries outside the USAT, BE, CH, CY, DE, DK, ES, FR, GB, IQ, IT, LB, NL, PA, PL, SA, SE, UY, ZA
Model numbers8780, 8781, 8784

Product

Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision Kit, model 8784. The Ascenda Intrathecal Catheter is part of an infusion system that stores and delivers parenteral drugs to the intrathecal space. The implanted infusion system components consist of a Medtronic pump and an Ascenda Intrathecal Catheter.

Reason for recall

Medtronic is removing specific lots of the Ascenda Intrathecal Catheters and Revision Kits, which are used with the implantable SynchroMed drug infusion pump. This recall is being conducted due to a single component of the catheter, the retainer ring, not meeting specification criteria. There is a possibility of unintentional disconnection of the catheter from the pump, or difficulty in disconne

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2172-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.