Monoject 0.9% Sodium Chloride Flush Syringe recall
Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing…
Why was Monoject 0.9% Sodium Chloride Flush Syringe recalled?
Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
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?
20I1524 20D0694 20I1584
- Product
- Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing…
- Recalling firm
- Cardinal Health
- Quantity
- 267,217,860 eaches in total
- Distribution
- US Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY.
- Recall date
- September 1, 2021
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)