ICU Recalls — U.S. Recall Records

Recall history in this database

Classification mix: Class II: 9.

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2683-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2681-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2676-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2679-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2680-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2682-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2678-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2677-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Medical DeviceJul 19, 2017

ICU The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise recall — FDA Z-2675-2017

A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

Class IIFDA: TerminatedICU

Understanding this recall history

This page summarizes recall records in which the official source identifies ICU 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.