FDA recall record

ICU Medical ASM Replacement Battery, Component Number SUB0000594 recall — FDA Z-1568-2023

Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than…

Class Iclassification
Z-1568-2023official record ID
May 24, 2023report date

Recall record at a glance

Official recordZ-1568-2023
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmICU Medical Inc.
Report dateMay 24, 2023
Recall initiation dateMar 22, 2023
Quantity344 units
LocationLake Forest, IL, United States

Official product description

ASM Replacement Battery, Component Number SUB0000594

Why the product was recalled

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 information

worldwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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