Medline EYE TRAY-LF Kits Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medline Industries is recalling 8 EYE TRAY-LF medical convenience kits because they contain mislabeled syringes.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 23, 2026 and geographically references California. Its severity classification of "medium" 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
Medline Industries, LP is recalling specific medical convenience kits because they contain Cardinal Health Monoject 1mL Luer Lock Syringes that are incorrectly labeled. The outer carton and blister pack state the syringes are 1 mL Luer Lock Tuberculin Syringes, but the contents are actually U-100 insulin syringes.
Which Products Are Affected
- Product: Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
- Quantity: 8 kits
- Lot Numbers: 26BMC538
- UDI/DI: 10198459151569 (each), 40198459151560 (case)
- Distribution: US Nationwide distribution in the states of California
- Recall Number: Z-2260-2026
- Classification: Class II
What You Should Do
Consumers should follow instructions provided in the recall notification from Medline Industries, LP.
Why This Matters
The mislabeling of syringe contents in these kits may lead to medication dosing errors.
Source
FDA recall Z-2260-2026. https://www.fda.gov
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 (972 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to June 23, 2026.
Frequently Asked Questions
Common questions about this FDA recall.