ICU Medical recalls MicroClave Clear Neutral Connectors with a visible gap between housing due to manufacturing defect. Affected units have specific product numbers and lot numbers listed in the recall notice.
Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.
ICU Medical is recalling MicroClave Clear Neutral Connectors because a manufacturing defect creates a visible gap between the connector's top and bottom housing. This gap could potentially lead to improper connections during medical procedures, though the recall does not specify a direct injury risk.
The connector has a visible gap between its top and bottom housing due to a manufacturing defect. This gap could cause improper connections when used with intravascular catheters, potentially leading to complications during medical procedures.
Healthcare professionals using intravascular catheters in medical settings are most likely affected. Patients receiving treatments through these connectors may be at risk if the connector malfunctions.
Check for product numbers MC100, MC100-PR, MC330446, or MC330545 with specific lot numbers listed in the recall notice. The UDI codes and lot numbers are provided in the recall details.
Identify the product number and lot numbers from the recall notice to confirm if your connector is affected.
The recall does not state that the connector is unsafe; it indicates a potential issue with the housing gap that may require verification.
The recall does not specify a remedy, so no action is required unless you have the affected product numbers and lot numbers listed.
Check the product number and lot numbers against the list provided in the recall notice.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1719-2022 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1719-2022 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
