Z-1956-2019 Class I Terminated
FDA device recall Z-1956-2019 was initiated by Centurion Medical Products Corporation on June 7, 2019 and is designated Class I. Reason for recall: Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube. The recall status is terminated (terminated July 28, 2020). Affected quantity: 80 kits.
Recall Details
- Product Type
- Devices
- Report Date
- August 7, 2019
- Initiation Date
- June 7, 2019
- Termination Date
- July 28, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 80 kits
Product Description
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Reason for Recall
Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.
Distribution Pattern
Distributed to one account in Arkansas.
Code Information
Lot 2018110290