Intersurgical recalls specific Superset airway connectors due to potential port cracks that could leak. Affected units include lot numbers 2180531, 2181808, 2182241, 2182533.
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 certain Superset airway connectors that may crack in the swivel elbow area, potentially causing leaks. This could lead to airway issues during medical procedures if not addressed.
The port in the swivel elbow section may crack when the flip cap is inserted. If the crack grows large enough, it could allow air or fluid to leak, potentially causing complications during medical procedures.
Medical professionals using the recalled Superset airway connectors for bronchoscopy procedures are most at risk. Patients undergoing these procedures with the affected connectors could experience leaks.
Check for the product name 'Superset' with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Affected units have lot numbers 2180531, 2181808, 2182241, or 2182533.
Identify the lot number on the connector to determine if it is affected (2180531, 2181808, 2182241, or 2182533).
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.
Check the lot number on the connector to see if it is affected (2180531, 2181808, 2182241, or 2182533). If affected, contact Intersurgical for guidance.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0786-2020 — Intersurgical Intersurgical Hello, I own a Intersurgical that is covered by recall Z-0786-2020 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.
