Recall Z-0149-2024— Cardinal Health 200, LLC
Class I · Ongoing
Class I FDA medical device recall by Cardinal Health 200, LLC, initiated 2023-09-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack. Reason: Demonstrated recognition and compatibility issues with syringe infusion pumps..
- Recalling firm
- Cardinal Health 200, LLC
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2023-09-20
- Firm location
- Waukegan, IL, United States
Product description
Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack
Reason for recall
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Data sourced from openFDA. This site is unofficial and independent of the FDA.