Argon Medical Devices Bone Marrow Tray Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Argon Medical Devices, Inc. is recalling 680 Bone Marrow Trays distributed nationwide due to potential sterility issues from included lidocaine ampules.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 11, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Argon Medical Devices, Inc. initiated a voluntary recall of certain Bone Marrow Trays because the kits contain Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall and do not meet release criteria for sterility.
Which Products Are Affected
Bone Marrow Tray, REF: CB0033TL and CB0355TLA. Affected lots include: CB0033TL (lots 11650820 and 11652276, expiration 3/31/2028) and CB0355TLA (lot 11651977, expiration 3/31/2028). A total of 680 units were distributed US nationwide including Puerto Rico, and to Trinidad and Tobago. Recall number Z-2709-2026. Classification: Class I.
What You Should Do
Consumers and healthcare providers should stop using the affected products and contact Argon Medical Devices, Inc. regarding the recall.
Why This Matters
The recall addresses a sterility concern in medical devices distributed across the United States and Puerto Rico.
Source
FDA recall Z-2709-2026 (event ID 99069)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (967 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 11, 2026.
Frequently Asked Questions
Common questions about this FDA recall.