Reported Jul 22, 2026 · Ongoing
T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL
Argon Medical Devices, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Argon Medical Devices, Inc · 1445 Flat Creek Rd · Athens, TX · 75751-5002
Is this the product you have?
- T-Lok Bone Marrow Tray
- REF
BMT1104STLBMET1104TLBMT1104CATL
- Lot codes and dates
3 of 3 products
Products covered by this recall # Barcodes Product as published 1 2088633300786200886333007868BMT1104STL/20886333007862:00886333007868/11650679(11/30/2026) 2 2088633300760200886333007608BMET1104TL/20886333007602:00886333007608/11654764(3/31/2028) 3 2088633300776300886333007769BMT1104CATL/20886333007763:00886333007769/11650887(11/30/2026) - Amount recalled
- 850
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Stop using this product now
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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