Data Foundry

Medical device recalls 2014

Sarns Soft-Flow Extended Aortic Cannulae 7 — Class II medical device recall Z-2099-2014

Terminated recall by Terumo Cardiovascular Systems Corporation, reported 2014-07-30, distributed nationwide. During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose f

Recall numberZ-2099-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTerumo Cardiovascular Systems Corporation, Ann Arbor, MI, United States
Recall initiated2014-05-23
Classified2014-07-22
Reported by FDA2014-07-30
Terminated2015-02-24
DistributedNationwide (US)
Countries outside the USAE, AU, BE, CA, CL, GB, JP, MX, MY, SG, TH, TW
Quantity135,340 units
Reason classesspecification failure
Lot numbers0645381, 0645876, 0646471, 0646532, 0648462, 0649394, 0650495, 0650731, 0651656, 0652314, 0652458, 0652909, 0653211, 0653430, 0655167, 0656442, 0656645, 0657280, 0658692, 0659823, 0660668, 0660743, 0661134, 0661526, 0661604, 0662071, 0666626, 0666665, 0667107, 0667247, 0667894, 0668568, 0668569, 0668979, 0669798, 0669799, 0669928, 0672089, 0672411, 0674021 and 88 more
Model numbers4948, 4949, 4949X, 4950, 4951, 4951X

Product

Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or without luer & Xcoating, Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.

Reason for recall

During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product specifications

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-2099-2014. 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.