Official recall notice
FDA DeviceClass INotable
FDA Recall: Arterial Line Kit 20ga x 6, REF: 400115A
- Recall date
- 2026-07-22
- Category
- Medical Device
- FDA class
- Class I
Why it was recalled
Hazard
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Product description
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Affected products
REF/UDI-DI Box:Unit/Lot(Expiration): 400115A/20886333212884:00886333212880/11655174(7/19/2027), 11655183(7/19/2027), 11655185(7/19/2027), 11659131(7/19/2027);