Medline Nerve Block Trays Recall (Z-2416-2026)
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 49,654 nerve block tray kits distributed nationwide because they contain a recalled adhesive lot and may have tubing that cracks during use.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 2, 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 block tray kits after determining they contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing may crack during actuation and render the product unusable for application.
Which Products Are Affected
- BLOCK TRAY DYNJRA2119A (UDI-DI 10198459194702, lot 25LBB738)
- INDWELLING NERVE BLOCK DYNJRA1011A (UDI-DI 10888277783614, lots 25KBB849 and 25LBB734) A total of 49,654 kits are affected. Distribution was to US Nationwide with OUS distribution pending. Recall number Z-2416-2026, Class II.
What You Should Do
Consumers should follow instructions provided in the recall notification from Medline Industries, LP.
Why This Matters
The recall affects nearly 50,000 kits distributed across the United States, potentially impacting availability of nerve block procedures.
Source
FDA recall Z-2416-2026, report date 20260624.
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 (952 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.