Fresh Recalls

FDAClass II · Medical device · Recall Z-2759-2026 · Recalled July 29, 2026

Hotline Fluid Warming Set recall — ICU Medical Inc.

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Hotline Fluid Warming Set
Company / brand
ICU Medical
Lot / serial / date codes
UDI-DI: 30695085407007; Lot Numbers: 4293568, 4293569, 4297510, 4297509, 4326087, 4337724, 4337725, 4346349
Distribution
Worldwide - US Nationwide distribution.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Hotline Fluid Warming Set

3. Open the official notice or contact

Official recall ID
Z-2759-2026
Brand
ICU Medical
Classification
Class II
Units affected
39,750 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Minneapolis, MN, United States
Firm address
6000 Nathan Ln N, N/A, 55442-1690

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI: 30695085407007; Lot Numbers: 4293568, 4293569, 4297510, 4297509, 4326087, 4337724, 4337725, 4346349
Distribution
Worldwide - US Nationwide distribution.
Firm notified the public via
Letter
FDA event ID
99289
Recall initiated
June 24, 2026
FDA classified
July 17, 2026
FDA report date
July 29, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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