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ETHEX Corporation Issues Nationwide Voluntary Recall of Products
Date:1/28/2009

seudovent 400 Capsules (58177-096-04) Pseudovent Capsules (58177-045-04) Pseudovent PED Capsules (58177-046-04) Tri-Vent DM Syrup (58177-925-07) Tri-Vent DPC Liquid (58177-923-07) Tri-Vent HC Liquid (58177-920-07) Products Recalled to RETAIL PHARMACY Level: Hydromorphone HCl Tablets, 2mg (58177-620-04 & 620-11) Hydromorphone HCl Tablets, 4mg (58177-621-04 & 621-11) Hydromorphone HCl Tablets, 8mg (58177-449-04) Metoprolol Succinate ER Tablets, 50mg (58177-369-04, 369-09 & 369-11) Metoprolol Succinate ER Tablets, 100mg (58177-368-04, 368-09 & 368-11) Metoprolol Succinate ER Tablets, 25mg (58177-293-04, 293-09 & 293-11) Metoprolol Succinate ER Tablets, 200mg (58177-358-04, 358-09 & 358-11)

Any wholesale or retail customer inquiries related to this action should be addressed to ETHEX Customer Service at 1-800-748-1472, faxed to ETHEX Customer Service at 314-646-3788, or e-mailed to customer-service@ethex.com. Representatives are available Monday through Friday, 8 am to 5 pm CST.

ETHEX Corporation has initiated recall notifications to wholesalers (and to retailers for Hydromorphone HCl and Metoprolol Succinate only) nationwide who received any inventory of the recalled products with instructions for returning the recalled products. Patients with questions about the recall should call the telephone number above, or contact their health-care providers.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA). At this time, the company is unable to determine when distribution of these products will resume.

Any adverse reactions experienced with the use of these products should also be reported to the FDA's MedWatch Pro
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SOURCE KV Pharmaceutical
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