Medline WMC I D PACK-LF Convenience Kits Recall
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Medline Industries, LP is recalling 32 units of WMC I D PACK-LF kits (model DYNJ50806L, lot 23FBK937) due to potential sterility assurance issues from sterilization equipment calibration problems.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 25, 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 has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Which Products Are Affected
Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L, UDI-DI: 10195327344672 (each), 40195327344673 (case), Lot Number: 23FBK937. Quantity: 32 units. Distribution: US Nationwide and worldwide.
What You Should Do
The recall was initiated voluntarily by the firm via letter on January 7, 2026.
Why This Matters
The potential impact on the sterility assurance level (SAL) of the recalled devices could affect product safety.
Source
FDA recall number Z-2119-2026, event ID 98642. Recalling firm: Medline Industries, LP, Northfield, IL.
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 (936 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 25, 2026.
Frequently Asked Questions
Common questions about this FDA recall.