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<p>[QUOTE="Anonymous, post: 3970549"]Novartis , Putting patients 1st , ALWAYS !!!</p><p><br /></p><p><br /></p><p>CIBA Vision O2 OPTIX contact lens recall</p><p>posted Monday 26th, February 2007 </p><p>defect on certain lots of the lenses could potentially harm the eye </p><p>We are taking this action because we have identified that some lenses in these lots did not meet our standards for ion permeability, a material characteristic which contributes to lens movement on the eye. </p><p>these lenses may cause persistent discomfort and/or foreign body irritation, and superficial corneal staining may be observed.</p><p><br /></p><p><br /></p><p><br /></p><p>Sandoz Inc. announced on October 26, 2010 that it is initiating a voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Sandoz and Parenta brand Methotrexate Injection, USP product (“methotrexate”) to the consumer/user level. Consistent with its commitment to quality and patient safety, Sandoz is initiating this voluntary recall of all 24 lots of the affected product following the finding of small glass flakes by Sandoz quality control in a limited number of vials and lots.</p><p><br /></p><p><br /></p><p>Sandoz Metoprolol Succinate ER Tablets Recall Has Been Done Rather Quietly </p><p>Many Patients Are Dissatisfied With Lack Of Information From Sandoz, FDA, Or Their Pharmacy About Why This Generic Toprol Pill Was Pulled </p><p>(Posted by Tom Lamb at DrugInjuryWatch.com) </p><p>In an August 26, 2008 Drug Injury Watch post, "FDA Warns Sandoz About Possible Quality-Control Problems At Its North Carolina Generic Drug Manufacturing Facility", I reported FDA inspectors found that Sandoz had failed to properly validate its manufacturing process for Metoprolol Succinate ER Tablets (Generic Form Of Toprol </p><p><br /></p><p>Sandoz Fentanyl Patch Recall</p><p>June 26, 2009 </p><p>If you or a member of your family have utilized the Sandoz fentanyl patch you need to be aware that there has been a recall of this product. Through this article you are provided a general overview of the circumstances and facts surrounding the Sandoz fentanyl patch recall. Armed with this information, you will be in the best possible position to understand your rights and what remedies are available to you incident to the Sandoz fentanyl patch recall. </p><p>The Sandoz fentanyl patch recall was issued as the result of a defect discovered in the product</p><p><br /></p><p><br /></p><p>Sandoz Inc. Recalls Several Lots of Lorazepam Tablets</p><p>What does this mean?</p><p>This recall for Lorazepam Tablets, USP, 0.5 mg, 1 mg, and 2 mg from Sandoz Inc. was issued at a warehouse and pharmacy level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you take Lorazepam and are concerned, you should speak to your doctor.</p><p>Sandoz Inc. is recalling several lots of Lorazepam Tablets, USP, 0.5 mg, 1 mg, and 2 mg because the lots did not pass the manufacturer's routine tests for quality and expiration dating. </p><p>Lorazepam is used in the treatment of anxiety. Lorazepam is also sold under the brand name Ativan. </p><p>To view the FDA notice about this recall and a complete list of recalled lot numbers, please visit:</p><p>more information here</p><p>Source: FDA</p><p>Publication Date: 2011-01-10[/QUOTE]</p><p><br /></p>
[QUOTE="Anonymous, post: 3970549"]Novartis , Putting patients 1st , ALWAYS !!! CIBA Vision O2 OPTIX contact lens recall posted Monday 26th, February 2007 defect on certain lots of the lenses could potentially harm the eye We are taking this action because we have identified that some lenses in these lots did not meet our standards for ion permeability, a material characteristic which contributes to lens movement on the eye. these lenses may cause persistent discomfort and/or foreign body irritation, and superficial corneal staining may be observed. Sandoz Inc. announced on October 26, 2010 that it is initiating a voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Sandoz and Parenta brand Methotrexate Injection, USP product (“methotrexate”) to the consumer/user level. Consistent with its commitment to quality and patient safety, Sandoz is initiating this voluntary recall of all 24 lots of the affected product following the finding of small glass flakes by Sandoz quality control in a limited number of vials and lots. Sandoz Metoprolol Succinate ER Tablets Recall Has Been Done Rather Quietly Many Patients Are Dissatisfied With Lack Of Information From Sandoz, FDA, Or Their Pharmacy About Why This Generic Toprol Pill Was Pulled (Posted by Tom Lamb at DrugInjuryWatch.com) In an August 26, 2008 Drug Injury Watch post, "FDA Warns Sandoz About Possible Quality-Control Problems At Its North Carolina Generic Drug Manufacturing Facility", I reported FDA inspectors found that Sandoz had failed to properly validate its manufacturing process for Metoprolol Succinate ER Tablets (Generic Form Of Toprol Sandoz Fentanyl Patch Recall June 26, 2009 If you or a member of your family have utilized the Sandoz fentanyl patch you need to be aware that there has been a recall of this product. Through this article you are provided a general overview of the circumstances and facts surrounding the Sandoz fentanyl patch recall. Armed with this information, you will be in the best possible position to understand your rights and what remedies are available to you incident to the Sandoz fentanyl patch recall. The Sandoz fentanyl patch recall was issued as the result of a defect discovered in the product Sandoz Inc. Recalls Several Lots of Lorazepam Tablets What does this mean? This recall for Lorazepam Tablets, USP, 0.5 mg, 1 mg, and 2 mg from Sandoz Inc. was issued at a warehouse and pharmacy level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you take Lorazepam and are concerned, you should speak to your doctor. Sandoz Inc. is recalling several lots of Lorazepam Tablets, USP, 0.5 mg, 1 mg, and 2 mg because the lots did not pass the manufacturer's routine tests for quality and expiration dating. Lorazepam is used in the treatment of anxiety. Lorazepam is also sold under the brand name Ativan. To view the FDA notice about this recall and a complete list of recalled lot numbers, please visit: more information here Source: FDA Publication Date: 2011-01-10[/QUOTE]
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Cafepharma Message Boards | Pharma Sales, Device Sales, Lab Sales
Home
Forums
>
Pharma/Biotech Companies
>
Novartis
>
Novartis milestones be proud ! Management take a bow !
>
Cafepharma Message Boards | Pharma Sales, Device Sales, Lab Sales
Home
Forums
>
Pharma/Biotech Companies
>
Novartis
>
Novartis milestones be proud ! Management take a bow !
>