Z-1566-2023 Class I Ongoing

Recalled by ICU Medical Inc — Lake Forest, IL

FDA device recall Z-1566-2023 was initiated by ICU Medical Inc on March 22, 2023 and is designated Class I. Reason for recall: Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease ea… The recall status is ongoing. Affected quantity: 23815 units.

Recall Details

Product Type
Devices
Report Date
May 24, 2023
Initiation Date
March 22, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
23815 units

Product Description

Replacement Battery List Number SUB0000594 found in Plum A+ & Plum A+3 Infusion Systems, List Numbers: a) 11005, b) 11971, c) 12391, d) 12618, e) 20678, f) 20679, g) 20792, h) 60629, i) 12348, j) 11973

Reason for Recall

Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease earlier in the battery lifecycle than expected.

Distribution Pattern

worldwide

Code Information

All devices containing CSB BATTERY displaying the first two (2) characters as 22 or lower