Intersurgical Double Swivel Elbow Airway Connector Recall: Port Crack Risk

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Recalling firmIntersurgical Inc6757 Kinne St, N/A · East Syracuse, NY 13057-1215

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Intersurgical is recalling a specific airway connector model because cracks in the port could leak. This risk is for medical devices used during bronchoscopy procedures.

Why it’s dangerous

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 complications during procedures.

Who’s affected

Medical professionals using this airway connector during bronchoscopy procedures. Patients using the device under medical supervision are at minimal risk.

How to tell if you have this one

Check for the model name 'Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1996030' and lot numbers 2180448, 2180742, or 2181001.

Brand
Intersurgical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers 2180448, 2180742, or 2181001 on the device.

✎ GovInfoNow

Questions people ask

Is this product dangerous if used properly?

The recall states the port may crack, but the device is safe if no cracks are present. Intersurgical does not specify if cracks occur under normal use.

What should I do if I have this product?

Intersurgical does not provide a remedy, so no action is required unless you find cracks in the port.

How can I tell if my product is affected?

Check for the model name and lot numbers listed: 2180448, 2180742, or 2181001.

Take action

Contact Intersurgical

We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0785-2020 — Intersurgical Intersurgical

Hello,

I own a Intersurgical that is covered by recall Z-0785-2020 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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Where this comes from

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.

Official source: FDA Recall #Z-0785-2020 (August 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0785-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Intersurgical Inc recalls Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1996030. Airway connector.

Lower-risk recall