ICU Medical Recalls Smiths ProPort Implantable Ports Over Safety Risks

ICU Medical’s Smiths business has recalled ProPort implantable ports due to a manufacturing defect that may cause the plastic port housing to separate from the reservoir, potentially leading to serious health risks.

Key Recall Details:

• Reason: Risk of housing detachment, which may cause air embolism, therapy interruption, or death.
• Action Required: Customers must stop using and return affected devices.
• Patient Monitoring: Clinicians should check for stability when palpating the port.

Additional Endotracheal Tube Recall

Smiths also warned of size discrepancies in certain oral/nasal endotracheal tubes (2.0-3.5 mm sizes). These may be smaller than expected, potentially leading to inadequate oxygen supply, underdose, or cardiopulmonary collapse.

ICU Medical, which acquired Smiths in 2022, continues to address quality system issues inherited from the purchase.

22-03-2025

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