Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2806-2018Class II

Kit w/3 Ext Sets, 3 Drop-In MicroClave Clear

ICU MEDICAL de MEXICO, S. de R.L. de C.V. / initiated 2018-03-01 / Terminated

ICU Medical de Mexico, S.A. de C.V. began a recall of Kit w/3 Ext Sets, 3 Drop-In MicroClave Clear on . FDA classified it as Class II and gives the reason as "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...". As of , the recall status on record is Terminated.

Recall record

Recall number
Z-2806-2018
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
ICU MEDICAL de MEXICO, S. de R.L. de C.V.
Product
Kit w/3 Ext Sets, 3 Drop-In MicroClave Clear
Product code
FMG Stopcock, I.V. Set
Reason for recall
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.
FDA root cause
Other
Action
ICU Medical notified customers of the recall on about 03/01/2018 via URGENT: Medical Device Recall Notification. The notification informed customers that this was an update and expansion to previously initiated recall. Instructions included to inspect inventory for affected devices, arrange for the return of affected devices, and complete and return the Urgent Medical Device Recall Notification Response Form to [email protected].
Quantity in commerce
302 pouches
Distribution
US distribution to AZ, MA, NC, OH, TX, VA, WA. Worldwide distribution to Belgium, France, Germany.
Product codes and lots
Item Number 011-AM6123.   a. Lot Number 3393136, UDI Number (01) 1 0840619 09404 8 (17) 220101 (30) 20 (10) 3393136, Expiration Date 11/01/2022;  b. Lot Number 3508527, UDI Number (01) 1 0840619 09404 8 (17) 220801 (30) 20 (10) 3508527, Expiration Date 08/01/2022

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2806-2018
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2797-2018Class IITerminatedVoluntary: Firm initiated
Z-2798-2018Class IITerminatedVoluntary: Firm initiated
Z-2799-2018Class IITerminatedVoluntary: Firm initiated
Z-2800-2018Class IITerminatedVoluntary: Firm initiated
Z-2801-2018Class IITerminatedVoluntary: Firm initiated
Z-2802-2018Class IITerminatedVoluntary: Firm initiated
Z-2803-2018Class IITerminatedVoluntary: Firm initiated
Z-2804-2018Class IITerminatedVoluntary: Firm initiated
Z-2805-2018Class IITerminatedVoluntary: Firm initiated
Z-2806-2018Class IITerminatedVoluntary: Firm initiated
Z-2807-2018Class IITerminatedVoluntary: Firm initiated
Z-2808-2018Class IITerminatedVoluntary: Firm initiated
Z-2809-2018Class IITerminatedVoluntary: Firm initiated
Z-2810-2018Class IITerminatedVoluntary: Firm initiated
Z-2811-2018Class IITerminatedVoluntary: Firm initiated
Z-2812-2018Class IITerminatedVoluntary: Firm initiated
Z-2813-2018Class IITerminatedVoluntary: Firm initiated
Z-2814-2018Class IITerminatedVoluntary: Firm initiated
Z-2815-2018Class IITerminatedVoluntary: Firm initiated
Z-2816-2018Class IITerminatedVoluntary: Firm initiated