ICU Medical de Mexico, S.A. de C.V. Recalls

Recall history in this database

Classification mix: Class II: 20.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 38 cm (15") Smallbore Ext Set w/6-Port NanoClave recall — FDA Z-2810-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V PROXIMALE - 18 cm (7") Appx 0.92 ml, PUR Smallbore Ext recall — FDA Z-2809-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 40 cm (16") Smallbore Ext Set w/6-Port NanoClave recall — FDA Z-2808-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 191 cm (75") Appx 2.9 ml, PVC/PUR Smallbore Bifuse Ext recall — FDA Z-2807-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 20 cm (8") PUR Smallbore Ext Set w/3-Port NanoClave recall — FDA Z-2797-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 10" Smallbore Ext Set w/6-Port NanoClave Manifold recall — FDA Z-2812-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 10" Smallbore Ext Set w/6-Port NanoClave Manifold, Check recall — FDA Z-2813-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V DISTALE - 203 cm (80") Bifuse Ext Set w/6 Gang 1o2 recall — FDA Z-2800-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave recall — FDA Z-2798-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave recall — FDA Z-2803-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V Kit w/3 Ext Sets, 3 Drop-In MicroClave Clear recall — FDA Z-2806-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port recall — FDA Z-2801-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 61 cm (24") Smallbore Ext Set w/6-Port NanoClave recall — FDA Z-2811-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 43 cm (17") Smallbore Ext Set w/3-Port NanoClave recall — FDA Z-2802-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 10" Smallbore Ext Set w/6-Port NanoClave Manifold recall — FDA Z-2815-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 30 cm (12") PUR Bifuse Ext Set w/3-Port NanoClave recall — FDA Z-2799-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-Port recall — FDA Z-2805-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 11" Smallbore Ext Set w/NanoClave, 6-Port NanoClave recall — FDA Z-2814-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave recall — FDA Z-2804-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Medical DeviceAug 22, 2018

ICU Medical de Mexico, S.A. de C.V 6" Smallbore Ext Set w/6-Port NanoClave Manifold, Check recall — FDA Z-2816-2018

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…

Class IIFDA: TerminatedICU Medical de Mexico, S.A. de C.V.

Understanding this recall history

This page summarizes recall records in which the official source identifies ICU Medical de Mexico, S.A. de C.V. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.