The FDA recently announced an immediate product recall of Sigma Spectrum Infusion Pumps. The recall affects pumps with model numbers 35700BAX and 35700ABB that were manufactured between July 1, 2005 and January 15, 2014.
The Spectrum Infusion Pump is a medical product widely used by hospitals and home health care professionals. It is used to administer intravenous fluids into a patient’s vein, artery, or spine, or under the skin. Intravenous fluids can include blood, saline, or medicine.
The ...
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Recently, the U.S. Food and Drug Administration issued a news release warning the public of a voluntary nationwide recall of one lot of 1% Lidocaine HCL Injection. Hospira, Inc., the product manufacturer as well as the world’s largest provider of injectable drugs, has issued this recall due to the presence oxidized stainless steel found in the drug particulates.