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ROi CPS LLC recalls Regard Custom Procedure Kits containing BD Luer Lok Access Devices
Recalled April 6, 2022 · FDA recall Z-0837-2022 · ROi CPS
Hazard
Recalled devices were packaged in convenience kits. · FDA Class III
Units
1750 kits
Sold at
US Nationwide distribution in the state of Missouri.
Description
Recalled devices were packaged in convenience kits.
Product
Regard Custom Procedure Kits containing BD Luer Lok Access Devices
Manufacturer(s)
ROi CPS LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →