PetSmart (NASDAQ: PETM) is voluntarily recalling two Dentley’s Beef Hoof products for potential salmonella contamination.
On November 5, 2009, In Food and Drug Administration, By admin
On November 4, 2009, In Food and Drug Administration, By admin
The U.S.
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FDA Unveils Safe Use Initiative that Targets Preventable Harm from Medication Use
On November 4, 2009, In Food and Drug Administration, By admin
Kits recalled because the pediatric tracheal tubes were manufactured with an internal diameter smaller than indicated on the label.
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Centurion Medical Products – Premie Pack and Meconium Pack – Recall
On November 2, 2009, In Food and Drug Administration, By admin
The U.S.
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FDA, JIFSAN Travel to Bangladesh to Teach Seafood Safety
On November 2, 2009, In Food and Drug Administration, By admin
The U.S. Food and Drug Administration today published a guidance document that should help manufacturers develop diagnostic tests for the 2009 H1N1 influenza virus. Although there are not any FDA-approved or cleared tests that diagnose this specific infection, during this pandemic, manufacturers can submit a request to the FDA for an Emergency Use Authorization (EUA)
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FDA Publishes Guidance on Diagnostic Tests for 2009 H1N1 Influenza Virus
On November 2, 2009, In Food and Drug Administration, By admin
The U.S. Food and Drug Administration today acted on new safety information about possible kidney function problems, including kidney failure, in patients taking Byetta (exenatide), a drug used to treat Type 2 diabetes.
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FDA: Byetta Label Revised to Include Safety Information on Possible Kidney Problems
On October 31, 2009, In Food and Drug Administration, By admin
Pointe Scientific, Inc, Canton, MI is initiating a nationwide recall of all size kits of Liquid Glucose Hexokinase Reagent catalog number G7517. The reagents have been found to fail linearity at > 200mg/dL that results in inaccurate glucose values above this range.
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Pointe Scientific, Inc Expands Nationwide Recall of Liquid Glucose Hexokinase Reagent (G7517)
On October 30, 2009, In Food and Drug Administration, By admin
Nationwide recall of all size kits. The reagents have been found to fail linearity at > 200mg/dL that results in inaccurate glucose values above this range.
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Pointe Scientific Liquid Glucose Hexokinase Reagent – Recall
On October 30, 2009, In Food and Drug Administration, By admin
Pointe Scientific, Inc, Canton, MI is initiating a nationwide recall of all size kits of Liquid Glucose Hexokinase Reagent catalog number G7517. The reagents have been found to fail linearity at > 200mg/dL that results in inaccurate glucose values above this range.
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Pointe Scientific, Inc Issues Nationwide Recall of Liquid Glucose Hexokinase Reagent (G7517)