FDA Enforcement
Class II
Terminated
216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, MicroClave Clear, Clamp, Rotating Luer.
Recall: Z-2801-2018
·
Reported August 22, 2018
Enforcement
- Recall Number
- Z-2801-2018
- Event ID
- 80460
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- ICU Medical de Mexico, S.A. de C.V.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- August 22, 2018
- Initiation Date
- March 1, 2018
- Classification Date
- August 16, 2018
- Termination Date
- January 26, 2024
- Address
- Avenida Cuarzo 250, Ensenada, Ejido Maneadero, N/A, Mexico
Description
216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, MicroClave Clear, Clamp, Rotating Luer.
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.
Code Info
Item Number 011-AM3010. Lot Number 3424312, UDI Number (01) 1 0840619 09487 1 (17) 220301 (30) 50 (10) 3424312, Expiration Date 03/01/2022
Distribution
US distribution to AZ, MA, NC, OH, TX, VA, WA. Worldwide distribution to Belgium, France, Germany.
Quantity
50 pouches