Medline Convenience 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, LP is recalling 227 units of two Medline Convenience Kit models nationwide because they contain recalled anesthetic drugs with quality issues.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 5, 2026 and geographically references United States. Its severity classification of "high" 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 Medline Convenience Kits after determining that the kits contain Arrow Kits and Sets including Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP. These drugs were recalled due to quality issues identified during a recent FDA inspection of the supplier. The recall is classified as Class I.
Which Products Are Affected
The recall covers 227 units distributed nationwide under the following products:
- DYNJ905503F (Model: CV ANESTHESIA - ROOM SET UP), UDI-DI 10193489967272 (each), 40193489967273 (case), Lot 24GBR740
- DYNJ905503F, Lot 24JBP984
- DYNJ905503G (Model: CV ANESTHESIA - ROOM SET UP), UDI-DI 10198459200397 (each), 40198459200398 (case), Lots: 26DBJ110, 25ABJ069, 25ABL749, 25CBB762, 25DBG799, 25EBM994, 25GBW226, 25LBA950, 25LBT019, 26ABH519, 26ABT315, 26BBQ338 Recall number Z-2452-2026. Recall initiation date: May 6, 2026.
What You Should Do
Consumers in possession of the affected kits should follow instructions provided in the firm's notification letter and contact Medline Industries, LP for further guidance.
Why This Matters
This Class I recall involves devices distributed across the United States that contain anesthetic products subject to quality concerns.
Source
FDA recall Z-2452-2026, report date July 1, 2026.
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 (1,373 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 5, 2026.
Frequently Asked Questions
Common questions about this FDA recall.