Medline BLOCK TRAY 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 270 BLOCK TRAY convenience kits nationwide due to quality issues with contained Lidocaine ampules.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 7, 2026 and geographically references United States. 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 initiated a voluntary recall of certain convenience kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules after Huons Co., Ltd. issued a recall notice due to quality issues identified during an FDA manufacturing inspection.
Which Products Are Affected
The affected product is Medline Convenience Kits: BLOCK TRAY, Model Number DYNJRA1590, Lot Number 25JLA522. UDI-DI codes are 10193489284829 (each) and 40193489284820 (case). A total of 270 kits were distributed nationwide in the United States under recall number Z-2535-2026.
What You Should Do
Consumers should verify the lot number on any affected kits and contact the recalling firm for further instructions regarding returns or refunds.
Why This Matters
The Class II recall addresses potential quality issues in medical devices distributed across the United States.
Source
FDA recall Z-2535-2026, event ID 99162.
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 (948 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.