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Medical Device

Arterial Line Kit 20ga x 6, REF: 400115A

Recall date: 2026-07-22 · Source: FDA_DEVICE
Product
Arterial Line Kit 20ga x 6, REF: 400115A
Reason for recall
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Units affected
440
Description
Arterial Line Kit 20ga x 6, REF: 400115A
View official recall notice →