RecallRadar

FDA Device recall Z-2798-2018

165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a single use, sterile, non-pyrogenic…

On 2018-08-22 the FDA classified a Class II recall of 165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a single use, sterile, non-pyrogenic… by Icu Medical De Mexico, citing ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a le….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2798-2018
ClassificationClass II
Statusterminated
Initiated2018-03-01
Published2018-08-22
Last updated2026-09-13 11:54 UTC
CompanyIcu Medical De Mexico
DistributionAZ, MA, NC, OH, TX, VA, WA

Product

165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system.

Reason

ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.

Identifiers

code_infoItem Number 011-AM3003. Lot Number 3297342, UDI Number (01) 1 0840619 09275 1 (17) 210700 (30) 50 (10) 3597342, Expiration Date 07/01/2021.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2798-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.