Argon Medical Devices, Inc: Instrument, Biopsy
Recall Summary Argon Medical Devices is recalling T-Lok Bone Marrow Trays that contain Lidocaine HCL Injection ampules because the ampules failed sterility testing requirements. The affected trays were distributed nationwide across the United States, Puerto Rico, Trinidad and Tobago, and Washington D.C. This is a Class II recall.
- Recalling firm
- Argon Medical Devices, Inc
- Product
- T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL
- Reason
- Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-01
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d6a0029c-ae11-4453-9419-1c72b17fb885