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22, the U.S. Food and Drug Administration (FDA) issued a recall alert, instructing practitioners to stop using all 27 lots of Teva's ketamine

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Ketamine recall alert! The FDA has confirmed that Teva Animal Health's original ketamine recall has been expanded to include 7 private labels.

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FDA does not endorse either the product or the company. Teva Animal Health, Inc. expands a voluntary nationwide recall of Ketamine

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FOR IMMEDIATE RELEASE -- December 21, 2009 - Teva Animal Health, Inc. is expanding a nationwide voluntary recall of Ketamine

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Bioniche Pharma Receives FDA Approval For 10 mg/mL Strength Of Ketamine Hydrochloride Injection, USP - Bioniche Pharma.

Ketamine is an anesthetic previously used in the operating room and for emergency situations in As an adjunct, we are using clonidine, 0.1 mg (per FDA).

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By now, some of you have heard the news that two common animal drugs manufactured by Teva Animal Health have been recalled.

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The only explanation so far given as to just what's wrong with the recalled ketamine came in a press release issued by the FDA on Dec.

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On 12/22/09 the FDA issued this Press Release Teva Animal Health, Inc. expands a voluntary nationwide recall of Ketamine Hydrochloride

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Veterinarians should stop using the recalled ketamine injectable immediately and return all existing products to the distributor, FDA says.

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