Intersurgical recalls specific airway connectors due to potential port cracks that could leak. Affected models include REF 1898000 with lot numbers 2181793-2191327. Contact for replacement.
The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
Intersurgical is recalling a specific airway connector model that may crack at the port insertion point, potentially causing leaks. This could lead to airway issues during medical procedures if not addressed.
The port in the swivel elbow may crack where the flip cap is inserted. If cracks grow large enough, they could leak air or fluid, potentially causing breathing issues during medical procedures.
Medical professionals using this airway connector for bronchoscopy procedures are most at risk. Patients undergoing procedures with this device could be affected if the connector leaks.
Check for the model number REF 1898000 on the connector. Affected units have lot numbers 2181793, 2182007, 2182830, 2183105, 2183345, 2190034, 2190139, 2191204, or 2191327.
Look for lot numbers 2181793, 2182007, 2182830, 2183105, 2183345, 2190034, 2190139, 2191204, or 2191327 on the connector.
The port may crack at the insertion point where the flip cap is placed, which could lead to leaks if the crack grows large enough.
The recall record does not specify a remedy, so contact Intersurgical directly for guidance.
The recall indicates a potential leak risk, but the record does not mention serious injury or death. This is considered low risk.
We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0784-2020 — Intersurgical Intersurgical Hello, I own a Intersurgical that is covered by recall Z-0784-2020 from Intersurgical. 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.
