Data Foundry

Medical device recalls 2026

Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H… — Class II medical device recall Z-1686-2026

Ongoing recall by Mentor Texas, LP., reported 2026-04-08, distributed nationwide. Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Recall numberZ-1686-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMentor Texas, LP., Irving, TX, United States
Recall initiated2026-02-18
Classified2026-03-27
Reported by FDA2026-04-08
DistributedNationwide (US)
Countries outside the USAT, AU, BE, BG, CA, CH, CZ, DE, DK, ES, FI, FR, GB, HR, IE, IS, IT, NO, PK, PL, RO, SA, SE, SG, SI, SK, TW
Reason classesdevice malfunction
UPC / GTIN / UDI-DI10081317028151, 10081317028168, 10081317028175, 10081317028199, 10081317028243, 10081317028250, 10081317028267, 10081317028274

Product

Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc

Reason for recall

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

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-1686-2026. 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.