PlainRecalls
FDA Devices Moderate Class II Terminated

Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.

Reported: January 15, 2020 Initiated: August 7, 2019 #Z-0786-2020

Product Description

Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.

Reason for Recall

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.

Details

Recalling Firm
Intersurgical Inc
Units Affected
19,200 pieces
Distribution
US Nationwide
Location
East Syracuse, NY

Frequently Asked Questions

What product was recalled?
Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.. Recalled by Intersurgical Inc. Units affected: 19,200 pieces.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 15, 2020. Severity: Moderate. Recall number: Z-0786-2020.