Drug recall
Arterial Line Kit 20ga x 6, REF: 400115A
FDA recall event 99069 · Class I · Argon Medical Devices, Inc
Key facts
| Event ID | 99069 |
|---|---|
| Recall numbers | Z-2704-2026, Z-2705-2026, Z-2706-2026, Z-2707-2026, Z-2708-2026, Z-2709-2026 |
| Recalling firm | Argon Medical Devices, Inc |
| Product type | Devices |
| Products | Arterial Line Kit 20ga x 6, REF: 400115A, Bone Marrow Tray, REF: CB0033TL; CB0355TLA, General Biospy Tray, REF: GUTS1000, One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular, T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL and 1 more |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Jun 1, 2026 |
| Report date | Jul 22, 2026 |
| City | Athens |
| State | TX |
| Country | United States |
| FEI number | 1625425 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: