Recall of Medline Medical Convenience Kits Due to Connection Risk
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 60 medical convenience kits because of a potential risk that the syringe rotating adaptor may unwind, leading to loose connections or disconnections.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 23, 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, cpsc, Devices.
What Happened
Medline Industries, LP has identified a potential risk through post-market surveillance where the syringe rotating adaptor in their medical convenience kits may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold.
Which Products Are Affected
The affected products are Medline medical convenience kits, labeled as MINOR PLASTIC-LF, with Medline Kit SKU # DYNJ86596. The kits contain NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. A total of 60 kits are involved, with UDI/DI for each at 10195327656119 and for the case at 40195327656110. The affected lot numbers are 24FMI029 and 24DMK138. These products were distributed worldwide, including the United States nationwide, Puerto Rico, and countries such as Canada, Netherlands, Australia, Korea, Republic of, Sri Lanka, Pakistan, Japan, United Arab Emirates, Singapore, and Slovakia.
What You Should Do
Consumers who have the affected products should follow the recalling firm's instructions, as notifications have been initiated via methods including email, fax, letter, press release, telephone, or visit. Contact Medline Industries, LP for information on returns or refunds.
Why This Matters
This recall is classified as Class I by the FDA, indicating a high potential for serious adverse health consequences due to the risk of disconnections in medical devices during use.
Source
FDA recall notice Z-1723-2026
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 (1,461 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 23, 2026.
Frequently Asked Questions
Common questions about this FDA recall.