Data Foundry

Medical device recalls 2020

6 — Class II medical device recall Z-0193-2021

Terminated recall by ICU Medical, Inc., reported 2020-10-28, distributed nationwide. Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lo

Recall numberZ-0193-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmICU Medical, Inc., San Clemente, CA, United States
Recall initiated2020-07-06
Classified2020-10-22
Reported by FDA2020-10-28
Terminated2023-05-11
DistributedNationwide (US)
Countries outside the USBE, BR, CA, DE, FR, IE, JP, MX, PL, SA
Reason classespackaging
UPC / GTIN / UDI-DI10887709062525
Lot numbers4493389, 4537168, 4558455

Product

6.5" (17 cm) Appx 0.30 ml, Smallbore Pressure Infusion (400psig) Ext Set w/Remv MicroClave, NanoClave T-Connector, Purple Clamp, Rotating Luer. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709062525(17)250101(30)50(10)4558455; (01)10887709062525(17)241201(30)50(10)4537168; (01)10887709062525(17)241201(30)50(10)4493389. The high pressure extension set is a device used as conduit tubing to deliver fluids from an ~f electronic or manual injector and may also be used as connector tubing to provide a sterile fluid pathway between two devices.

Reason for recall

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

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-0193-2021. 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.