Regard Custom Procedure Kits containing BD Luer Lok Access Devices

Recall Insight

This FDA Devices action (record #Z-0837-2022) was formally reported on April 6, 2022, with the manufacturer initiating the action on February 24, 2022. It is classified under Low severity (Class III), with a current status of Terminated. ROi CPS LLC is listed as the recalling firm, operating out of Republic, MO. Federal records indicate 1750 kits units are affected.

The documented reason for this recall is: Recalled devices were packaged in convenience kits. Distribution data in the federal record shows the product reached: US Nationwide distribution in the state of Missouri.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 4 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.