CONTACT: TAMMY BUTLER THER-RX CORPORATION 877-567-7676 FOR IMMEDIATE RELEASE -- ST. LOUIS, MO, FEBRUARY 3, 2009 – THER-RX CORPORATION, A SUBSIDIARY OF KV PHARMACEUTICAL COMPANY IS ISSUING A VOLUNTARY NATIONWIDE RECALL OF PRESCRIPTION PRENATAL AND IRON SUPPLEMENT NUTRITIONALS AS IDENTIFIED BELOW (ALL LOTS WITHIN THEIR EXPIRATION DATES) AT A … [Read more...]
ETHEX Corporation Issues Nationwide Voluntary Recall of Products (January 28)
Click Here for previous ETHEX recalls ETHEX CORPORATION, A SUBSIDIARY OF KV PHARMACEUTICAL (NYSE: KVA/KVB), IS ISSUING, AS PREVIOUSLY DISCLOSED BY KV PHARMACEUTICAL COMPANY ON JANUARY 26, 2009, A NATIONWIDE VOLUNTARY RECALL OF THE PRODUCTS IDENTIFIED BELOW (ALL LOTS WITHIN THEIR EXPIRATION DATES) AT A WHOLESALE OR A RETAIL LEVEL AS A PRECAUTIONARY … [Read more...]
Ther-Rx Corporation Recalls Gynazole-1, Clindesse, Microk, Extencaps and Other Medications
CONTACT: TAMMY BUTLER, CUSTOMER SERVICE MANAGER 1-877-567-7676 FOR IMMEDIATE RELEASE -- ST. LOUIS, JAN. 28, 2009 – THER-RX CORPORATION, A SUBSIDIARY OF KV PHARMACEUTICAL (NYSE: KVA/KVB), IS ISSUING, AS PREVIOUSLY DISCLOSED BY KV PHARMACEUTICAL COMPANY ON JANUARY 26, 2009, A VOLUNTARY NATIONWIDE RECALL OF THE PRODUCTS IDENTIFIED BELOW (ALL … [Read more...]
FDA Announces Class I Recall of Ophthalmic Surgical Device
THE U.S. FOOD AND DRUG ADMINISTRATION ANNOUNCED A CLASS I RECALL OF LOT NO. UD30654 OF HEALON D, AN OPHTHALMIC VISCOSURGICAL DEVICE (OVD) MANUFACTURED BY ADVANCED MEDICAL OPTICS INC. (AMO) OF SANTA ANA, CALIF. OVDS ARE VISCOELASTIC MATERIALS USED TO MAINTAIN SPACE IN THE EYE DURING SURGERY. TYPICALLY, OVDS ARE PRE-PACKAGED IN A SYRINGE AND ARE … [Read more...]
Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile (December 23)
Stryker Craniomaxillofacial has issued a nationwide recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile Stryker's Craniomaxillofacial (CMF) business unit announced today that the U.S. Food and Drug Administration (FDA) concluded on Dec. 18, 2008 that its recall of the … [Read more...]
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