Medline Anesthesia Kit Recall Issued
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 1,400 ANESTHESIA KIT PEDS 90-LF units distributed nationwide due to inclusion of recalled temperature probes.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 9, 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 because they contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. that were subject to an error in Medtronic's distribution control process.
Which Products Are Affected
The affected product is the Medline Convenience Kit: ANESTHESIA KIT PEDS 90-LF, Model Number DYNJAP10125A. The recall covers 1400 kits with Lot Number 24JBR072 and UDI-DI 10198459112911 (each), 40198459112912 (case). Distribution was nationwide in the United States under FDA recall number Z-2695-2026, classified as Class II.
What You Should Do
Consumers should follow guidance from the recalling firm or the FDA regarding the ongoing recall.
Why This Matters
The recall affects 1,400 kits distributed across the United States and stems from an upstream distribution error involving the included temperature probes.
Source
https://www.fda.gov - FDA recall event ID 99196, report date 20260715
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 (1,020 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.