Medical device maker Covidien Plc said it was recalling 14 lots of its Monoject prefill flush syringes sold in the United States and Bermuda as they contained non-sterilized water which could cause life-threatening infections.
Some of the syringes, meant to administer saline or heparin, also had mismatched caps, labels and wrappers, the company said.
More information is available on the FDA website: http://www.fda.gov/Safety/Recalls/ucm365577.htm.
The syringes are used to reduce blood clots in veins and remove medication left at catheter sites.
Using the heparin syringe containing only water could cause clotting in catheters.
Reuters
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