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Urgent site urgencyFDA Class I

T-Lok Bone Marrow Tray, REF: BMT1104STL

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Agency
FDA Device
Recall date
Jun 1, 2026
Status
Ongoing
Company
Argon Medical Devices, Inc

1. What product was recalled?

Bone Marrow Tray, REF: CB0033TL

Bone Marrow Tray, REF: CB0033TL; CB0355TLA

Quantity: 680

Code or lot text: REF/UDI-DI Box:Unit/Lot(Expiration): CB0033TL/20886333217308:00886333217304/11650820(3/31/2028), 11652276(3/31/2028); CB0355TLA/20886333217698:00886333217694/11651977(3/31/2028);

LOT
11652276(3/31/2028)
LOT
CB0355TLA/20886333217698:00886333217694/11651977(3/31/2028)
LOT
REF/UDI-DI Box:Unit/Lot(Expiration): CB0033TL/20886333217308:00886333217304/11650820(3/31/2028)
RECALL-NUMBER
Z-2709-2026

T-Lok Bone Marrow Tray, REF: BMT1104STL

T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL

Quantity: 850

Code or lot text: REF/UDI-DI Box:Unit/Lot(Expiration): BMT1104STL/20886333007862:00886333007868/11650679(11/30/2026); BMET1104TL/20886333007602:00886333007608/11654764(3/31/2028); BMT1104CATL/20886333007763:00886333007769/11650887(11/30/2026)

LOT
BMET1104TL/20886333007602:00886333007608/11654764(3/31/2028)
LOT
BMT1104CATL/20886333007763:00886333007769/11650887(11/30/2026)
LOT
REF/UDI-DI Box:Unit/Lot(Expiration): BMT1104STL/20886333007862:00886333007868/11650679(11/30/2026)
RECALL-NUMBER
Z-2707-2026

2. Is my exact product affected?

Compare every printed identifier. A matching value can indicate that your product is included.

3. What is the hazard?

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

4. What should I do now?

Follow the FDA recall notice and contact the recalling company for current instructions.

5. Where was it sold or distributed?

Nationwide

View source evidence for state distribution
  • Puerto Rico: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.

6. Were injuries or illnesses reported?

No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.

7. What remedy is available?

Follow the FDA recall notice and contact the recalling company for current instructions.

8. Is the recall active or closed?

The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.

9. When was the information checked?

Last checked .

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10. Where is the official source?

Open the official FDA Device source

The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.