Monoject" recall
Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack
Why was Monoject" recalled?
Demonstrated recognition and compatibility issues with syringe infusion pumps.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product Code: 1186000777T; UDI/DI: 10192253025835 - each, 20192253025832 - box, 50192253025833 - case; Lot Numbers: 221101, 230601
- Product
- Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack
- Recalling firm
- Cardinal Health 200, LLC
- Quantity
- 457,200 units
- Distribution
- US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.
- Recall date
- November 1, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)