Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU Due to A possible interruption of therapy when an E321...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ICU directly.
Affected Products
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.
Quantity: 7351 units
Why Was This Recalled?
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ICU
ICU has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report