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Author Topic: De-wormer recalls  (Read 1655 times)
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RIP little angel Katey


« on: September 18, 2009, 12:51:26 PM »

I would think most vets would know about this, but shelters and pet stores might not.

PRODUCT
Praziquantel Injection, 56.8 mg/ml, ANDA 200-176, RX, packaged in 10-ml. vials under the following labels: (1) VEDCO Cestoved; (2) Butler Praziject; and (3) Phoenix Pharmaceutical Inc. CestaJect, Recall # V-270-2009
CODE
Lot 7060853, Exp. 6/2009
RECALLING FIRM/MANUFACTURER
TEVA Animal Health Inc., St. Joseph, MO, by letter dated May 15, 2009. Firm initiated recall is ongoing.
REASON
The product does not meet the appearance specification and was not manufactured in conformance with GMP’s.
VOLUME OF PRODUCT IN COMMERCE
5,475/10-ml. vials
DISTRIBUTION
Nationwide

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6) Praziquantel Tablets, 34 mg, RX, packaged under the following labels: (1) Trade Winds Tape Worm Tabs, packaged in 5-tab. bottles; (2) Farnam D-Worm Praziquantel Tablets, packaged in 5- and 10-tab. bottles; (3) Phoenix Pharmaceutical Inc. CestaTabs, packaged in 50- and 150-tab. bottles; (4) VEDCO Cestoved Tablets, packaged in 50- and 150-tab. bottles; (5) Butler Prazitabs D, packaged in 50- and 150-tab. bottles; and (6) AmTech Group Inc. Praziquantel Tablets, packaged in 50- and 150-tab. bottles, Recall # V-265-2009;
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My little babies, you'll always be in my heart. Mom will see you later. Look after each other, ok?
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