Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled by ROi CPS LLC Due to Recalled devices were packaged in convenience kits.

Date: February 24, 2022
Company: ROi CPS LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact ROi CPS LLC directly.

Affected Products

Regard Custom Procedure Kits containing BD Luer Lok Access Devices

Quantity: 1750 kits

Why Was This Recalled?

Recalled devices were packaged in convenience kits.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About ROi CPS LLC

ROi CPS LLC has 86 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report