Data Foundry

Medical device recalls 2020

60" — Class II medical device recall Z-0206-2021

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-0206-2021
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-DI10887709083889
Lot numbers4514845, 4549102, 4730714

Product

60" (152 cm) Appx 1.0 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, NanoClave, 0.2 Micron Filter, 1.2 Micron Filter, 4 Clamps (2 Blue, Yellow, White), Rotating Luer; 1 unit per pouch, 50 multivac pouches per case UDI:(01)10887709083889(17)241201(30)50(10)4514845; (01)10887709083889(17)250101(30)50(10)4549102; (01)10887709083889(17)250201(30)50(10)4730714. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patient's vascular system through the administration set's needle or catheter (which is inserted into a vein).

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-0206-2021. 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.