Intersurgical recalls specific Superset airway connectors due to potential port cracking in the swivel elbow that could leak. Affected units have lot numbers 2182536-2191591.
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 the leak occurs.
The port in the swivel elbow section may crack when the flip cap is inserted. If the crack grows large enough, it could leak air or fluid, potentially causing breathing issues 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 complications.
Check for the specific Superset airway connector with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Affected units have lot numbers 2182536, 2182852, 2183161, 2190350, 2190531, 2190617, 2191025, or 2191591.
Look for the lot numbers 2182536, 2182852, 2183161, 2190350, 2190531, 2190617, 2191025, or 2191591 on the connector.
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. If it matches the affected numbers, contact Intersurgical for further instructions.
The recall states that cracks could leak, but no specific injury mechanism is described. The risk level is low based on the information provided.
We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0787-2020 — Intersurgical Intersurgical Hello, I own a Intersurgical that is covered by recall Z-0787-2020 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.
