Z-1568-2023 Class I Ongoing

Recalled by ICU Medical Inc — Lake Forest, IL

FDA device recall Z-1568-2023 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: 344 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
344 units

Product Description

ASM Replacement Battery, Component Number SUB0000594

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

Lot Numbers: 5660479