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Open, Classified

Plum Duo Infusion System, List Number 40002-04-01

FDA Recall Z-1094-2026 · Posted 2026-01-15

Recalling FirmICU Medical, Inc.
Recall StatusOpen, Classified
Product CodeFRN
Date Initiated2025-12-15
Product Quantity423 units

Reason for Recall

ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo Infusion Pump fails, the pump may not produce audible alarms, alerts, or provide audible feedback for touchscreen inputs.

Firm Action

An URGENT: MEDICAL DEVICE CORRECTION dated 12/15/25 was sent to customers. Actions for Users: 1. Identify all affected infusion pumps in your possession and ensure all users or potential users of these pumps are immediately informed of this notice. If the devices are used at another location, please ensure this communication is delivered to that location. 2. If the primary speaker fails, obtain another pump to continue the infusion. Remove the affected pump from clinical use until the speaker can be replaced. 3. Complete and return the attached Customer Response Form to [email protected] within 10 days of receipt to acknowledge your understanding of this notification. 4. If you have distributed affected products to your customers, please immediately forward this notice to them. Request that they complete the response form and return it to [email protected]. Follow-up Actions by ICU Medical: ICU Medical will address the issue described in this letter through a software update. This update will ensure the backup buzzer will always generate audio for alarms, malfunctions and alerts. ICU Medical will contact you to schedule the software correction for this issue. Device Correction Inquiries https://icumed.custhelp.com/app/market-action For any questions regarding this action

Root Cause

Nonconforming Material/Component

Distribution Pattern

Worldwide - US Nationwide distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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