Z-2340-2026 Class II Ongoing
FDA device recall Z-2340-2026 was initiated by Avanos Medical, Inc. on April 30, 2026 and is designated Class II. Reason for recall: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. The recall status is ongoing. Affected quantity: 54 kits.
Recall Details
- Product Type
- Devices
- Report Date
- June 17, 2026
- Initiation Date
- April 30, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 54 kits
Product Description
Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No
Reason for Recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Distribution Pattern
US Nationwide distribution.
Code Information
UDI-DI 10350770007530, Lot Numbers 30365233, 30367015, 30372821, 30378386