- Recalling firm
- Avanos Medical, Inc.
- Reason for recall
- Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Affected products (lot / model / serial)
- UDI-DI 10350770007530, Lot Numbers 30365233, 30367015, 30372821, 30378386
- Units affected
- 54 kits
- Distribution pattern
- US Nationwide distribution.
- Firm location
- Alpharetta, GA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2340-2026
- Recall initiated
- April 30, 2026
- FDA classification date
- June 5, 2026
- FDA report date
- June 17, 2026
- FDA event ID
- 98907
- Last updated on HTM Vibe
- July 23, 2026