FDAClass IISeptember 18, 2013

Monoject 10 Units/mL Heparin Lock Flush recall: Sterility Concern

Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881580123 Product Usage: Both 0.9% Sodium Chloride Flush syringes…

Why was Monoject 10 Units/mL Heparin Lock Flush recalled?

Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

Lot Numbers: 13A0084N

Product
Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 3 mL Fill Product ID: 8881580123 Product Usage: Both 0.9% Sodium Chloride Flush syringes…
Recalling firm
Covidien LLC
Quantity
Unknown
Distribution
Worldwide Distribution - USA Nationwide and the country of Bermuda
Recall date
September 18, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls