Recall of See Luer Cap Set by Molded Products Inc
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Molded Products Inc. is voluntarily recalling 26,900 units of the See Luer Cap Set due to a confirmed complaint of the threaded sleeve not being engaged and becoming unattached.
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 "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
Molded Products Inc. is conducting a voluntary recall of the See Luer Cap Set because of a confirmed complaint that the threaded sleeve may not be engaged and could become unattached, potentially affecting its use as an intravascular administration set.
Which Products Are Affected
The affected product is the See Luer Cap Set, model MPC-130, described as a set for intravascular administration. The recall involves 26,900 units with code information including UDI +B144MPC1300/$529105203895 and Lot Number 20389. Distribution occurred nationwide in the United States, specifically in the states of TN, TX, NV, IL, and FL. The recall number is Z-1774-2026.
What You Should Do
Consumers should contact Molded Products Inc. at their address, 1812 Industrial Pkwy, Harlan, IA 51537-2401, as the recall was initiated via letter. Follow the instructions provided in the firm's notification for returns or refunds.
Why This Matters
This recall involves a medical device that could pose a risk if the threaded sleeve detaches, potentially impacting patient safety during use. It highlights the importance of ensuring device integrity in healthcare settings.
Source
Attribution: FDA Recall Notice, event ID 98469, reported on 20260415.
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 (1,255 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to April 23, 2026.
Frequently Asked Questions
Common questions about this FDA recall.