Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow conditions, List Number L-70
FDA Recall Z-2759-2026 · Posted 2026-07-17
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Recalling FirmICU Medical Inc.
Recall StatusOpen, Classified
Product CodeLGZ
Date Initiated2026-06-24
Product Quantity39,750 units
Reason for Recall
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return connector bond.
Firm Action
An URGENT: MEDICAL DEVICE CORRECTION notification letter dated 6/24/26 was sent to customers.
Actions for Users:
When using the device, all instructions, including warnings and cautions contained in the Instructions for Use must be followed with heightened awareness. Please complete the following actions below.
1. Locate potentially affected devices from the Lots listed in Table 1 above.
2. Destroy all affected products following your institution s process for destruction. If destroying is not immediately possible at your facility, then the product should be quarantined until disposal.
3. Share this notification with all potential users of the device to ensure they are aware of this notification. If the devices are used at another location, please ensure that this communication is delivered there.
4. Complete and return the attached Customer Response Form to [email protected] within 10 days of receipt to acknowledge your understanding of this notification.
Required Actions for Distributors:
When using the device, all instructions, including warnings and cautions contained in the Instructions for Use must be followed with heightened awareness. Please complete the following actions below.
1. Locate potentially affected devices from the Lots listed in Table 1 above.
2. Destroy all affected products following your institution s process for destruction. If destroying is not immediately possible at your facility, then the product should be quarantined until disposal.
3. Share this notification with all potential users of the device to ensure they are aware of this notification. If the devices are used at another location, please ensure that this communication is delivered there.
4. Complete and return the attached Customer Response Form to [email protected] within 10 days of receipt to acknowledge your understanding of this notification.
5. DISTRIBUTORS: Immediately forward this notice to all users to whom you distributed these products. IC
Root Cause
Process control
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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