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 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
Reported: September 18, 2013 Initiated: August 16, 2013 #Z-2182-2013
Product Description
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 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
Reason for Recall
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Details
- Recalling Firm
- Covidien LLC
- Units Affected
- Unknown
- Distribution
- Worldwide Distribution - USA Nationwide and the country of Bermuda
- Location
- Mansfield, MA
Frequently Asked Questions
What product was recalled? ▼
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 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. Recalled by Covidien LLC. Units affected: Unknown.
Why was this product recalled? ▼
Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 18, 2013. Severity: Moderate. Recall number: Z-2182-2013.
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