Data Foundry

Medical device recalls 2025

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial… — Class I medical device recall Z-2081-2025

Ongoing recall by Edwards Lifesciences, LLC, reported 2025-07-16, distributed nationwide. due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body

Recall numberZ-2081-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmEdwards Lifesciences, LLC, Irvine, CA, United States
Recall initiated2025-05-14
Classified2025-07-10
Reported by FDA2025-07-16
DistributedNationwide (US)
Countries outside the USAE, AT, AU, BE, BG, BR, CA, CH, CL, CO, CY, CZ, DE, DK, ES, FR, GB, GR, HU, IE, IL, IN, IS, IT, JP, KR, LU, MT, MX, MY, NL, NO, PA, PK, PL, PT, RO, SE, SG, SK, TH, TW, ZA
Quantity13,240
UPC / GTIN / UDI-DI00690103180565
Lot numbersBSLC9155
Serial numbers130451, 130466, 130472, 130593, 130709, 130764, 130818, 130821, 130847, 130948, 130952, 131038, 131043, 131047, 131182, 131193, 131231, 131236, 131289, 131311, 131317, 131433, 131435, 131513, 131516 and 59 more
Model numbersOPTI18

Product

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours. Component: No

Reason for recall

due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.

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-2081-2025. 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.