Z-1765-2019 Class I Terminated
FDA device recall Z-1765-2019 was initiated by Teleflex Medical on May 24, 2019 and is designated Class I. Reason for recall: This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector beco… The recall status is terminated (terminated February 15, 2022). Affected quantity: 77136 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 26, 2019
- Initiation Date
- May 24, 2019
- Termination Date
- February 15, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 77136 units
Product Description
Sheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management
Reason for Recall
This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.
Distribution Pattern
Worldwide - US Nationwide Distribution
Code Information
Lot Numbers: 73K1600156 73K1600735 73L1600501 73A1700120 73B1700321 73C1700425 73D1700630 73E1700504 73G1700146 73H1700053 73J1700307 73K1700085 73B1800223 73B1800371 73C1800372 73D1800655 73E1800579 73G1800627 73H1800203 73H1800429 73H1800758 73J1800118 73J1800696