Regard Custom Procedure Kits containing BD Luer Lok Access Devices
Reported: April 6, 2022 Initiated: February 24, 2022 #Z-0837-2022
Product Description
Regard Custom Procedure Kits containing BD Luer Lok Access Devices
Reason for Recall
Recalled devices were packaged in convenience kits.
Details
- Recalling Firm
- ROi CPS LLC
- Units Affected
- 1750 kits
- Distribution
- US Nationwide distribution in the state of Missouri.
- Location
- Republic, MO
Frequently Asked Questions
What product was recalled? ▼
Regard Custom Procedure Kits containing BD Luer Lok Access Devices. Recalled by ROi CPS LLC. Units affected: 1750 kits.
Why was this product recalled? ▼
Recalled devices were packaged in convenience kits.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 6, 2022. Severity: Low. Recall number: Z-0837-2022.
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