Argon Medical Devices
7 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Argon Medical Devices and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-07-22FDA-DeviceClass IArgon Medical bone marrow tray recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceClass IArgon Medical Arterial Line Kit recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceClass IArgon Medical T-Lok Bone Marrow Tray recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceClass IArgon Medical biopsy kit recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceClass IArgon Medical introducer trays recalled for sterility issue
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceClass IArgon Medical pacing electrode trays recalled for sterility risk
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2025-12-03FDA-DeviceClass IIOption"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary thromboembolism when anticoagulants are contraindicated " Failure of anticoagulant therapy in thromboembolic disease " Emergency treatment following massive pulmonary embolism where anticipated benefits of conventional t
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied
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