ICU Medical recalls specific batteries for Plum A+ and A+3 infusion systems that may lose capacity earlier than expected. Affected units include those with list numbers 11005 through 20792. Replace with new batteries to prevent unexpected shutdowns.
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.
ICU Medical is recalling certain batteries for Plum A+ and Plum A+3 infusion systems because they may lose capacity earlier than expected, leading to shorter battery life. This could cause the infusion system to shut down unexpectedly during use.
The batteries may lose capacity earlier than expected due to a manufacturing defect from the battery supplier. This can cause the infusion system to shut down unexpectedly, potentially interrupting treatment.
Patients using ICU Medical's Plum A+ or Plum A+3 infusion systems with specific battery list numbers are affected. Healthcare providers and patients using these systems are most at risk if the battery fails during treatment.
Check if your Plum A+ or Plum A+3 infusion system has a battery labeled with list numbers 11005 through 20792. Also, look for batteries with the first two characters as '22' or lower on the CSB battery label.
Look for the battery list number on the device or battery label to confirm if it's affected.
Contact ICU Medical to get a replacement battery for affected units.
The recall does not specify an immediate replacement deadline; contact ICU Medical for a replacement battery.
Affected batteries have list numbers 11005 through 20792, as listed in the recall notice.
Check the battery label for list numbers 11005 through 20792 or if the first two characters are '22' or lower.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1566-2023 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1566-2023 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
