Home / Recalls / Medical Devices
Covidien LLC recalls Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID:8881580121 Product Usage: Both 0.
Recalled September 18, 2013 · FDA recall Z-2181-2013 · Covidien
Hazard
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin · FDA Class II
Units
Unknown
Sold at
Worldwide Distribution - USA Nationwide and the country of Bermuda
Description
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Product
Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 10 mL Fill Product ID:8881580121 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible intravenous administration sets and indwelling intravenous access devices
Manufacturer(s)
Covidien LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →