ICU Medical recalls MicroClave Clear Neutral and Clear Connectors due to a visible gap between housing that may cause disconnection during medical use. Affected units have specific product numbers and lot numbers.
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 and Clear Connectors because a manufacturing defect creates a visible gap between the connector's top and bottom housing. This gap could lead to disconnection during intravenous medical procedures, potentially causing treatment interruptions.
A visible gap between the connector's top and bottom housing can cause the connector to disconnect during medical use. This disconnection could interrupt intravenous treatments, potentially delaying critical medical care.
Healthcare professionals using these connectors for intravenous administration sets are most at risk. Patients receiving IV treatments with the recalled connectors may experience treatment interruptions.
Check for product numbers: MR4001, MS984, or SC3000. Look for lot numbers: 5737404, 5740700-5740721, 5793254-5793259, 5738132, 5737492, 5726857, 5753967. These connectors are used in intravenous administration sets.
Identify your connector using the product numbers (MR4001, MS984, SC3000) and lot numbers listed in the recall notice.
A manufacturing defect causes a visible gap between the connector's top and bottom housing, which may lead to disconnection during medical use.
Check your product details against the list of affected units provided in the recall notice. No specific action is required beyond identifying the affected units.
The recall states a visible gap could cause disconnection during medical use, potentially interrupting intravenous treatments. However, no specific injury mechanism is described.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1722-2022 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1722-2022 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.
