Fda duragesic recall

Common Questions and Answers about Fda duragesic recall

duragesic

401095 tn?1351391770 Avis is wise. "Fentanyl is an opioid analgesic with a potency approximately eighty times that of morphine." According to the FDA: "Duragesic is to be used only for the management of severe, chronic pain (such as cancer pain) that cannot be managed with less powerful drugs such as acetaminophen-opioid combinations and nonsteroidal analgesics.
1916673 tn?1420233270 On April 22, 2015, the FDA announced that Nylabone Products of Neptune, New Jersey, is recalling one lot of its Puppy Starter Kit dog chews due to possible contamination with Salmonella bacteria. For more information, please follow this link: http://clicks.aweber.com/y/ct/?l=AeZ.
675347 tn?1365460645 The FDA has announced that Midwestern Pet Food is expanding its recent recall to include more brands and over 1000 lots of its dog and cat foods because they contain potentially deadly levels of aflatoxin. FDA is aware of at least 70 deaths and 80 illnesses in dogs who ate the affected products. For full details, please visit the following link: https://www.dogfoodadvisor.
566175 tn?1278430472 And even if you have peanut butter products that arent included in the recall, it still may be a good idea to throw out any thing that you're not sure about. Taking care of our September mommies and babies!!
390388 tn?1279636213 I hit the button to fast to post. On the FDA site they have a place where you can be notified of any recalls listed; "after the dog food recalls" I had put my email address in to be notified of any updated recalls and never got off the list. Its hard to believe all the things that get recalled and never brought to attention to the people. It's free for anyone to get on. Just thought I would pass it along.
Avatar f tn t know if they still are but earlier the website was having technical issues and it was saying that ANY lot number you put in was not part of the recall. I followed the link on the main recall page that gives you a pdf of ALL lot numbers that are part of it just to be safe because we use Similac too. The can I've been using isn't listed but I'm still scared to use it.
564735 tn?1263943526 I was just wondering if anyone has used duragesic pain patches. My oncologist is recommending I use these patches from ongoing pain from tumors. I am a little nervous about using the patches but I am also over the pain. The pain has restricted my lifestyle. Going to go the grocery store or running errands has become difficult and I am no longer able to go to the gym. Has anyone had problems with these patches? If you used the patches, how long did you use them?
Avatar f tn By Parija Kavilanz, senior writerMay 14, 2010: 8:28 PM ET NEW YORK (CNNMoney.com) -- The quality and safety violations that led to the shutdown of a Tylenol plant were extremely serious, and could lead to tough action by regulators on drugmaker Johnson & Johnson.
82861 tn?1333453911 Me967 just sent me this information from the FDA. Thanks!
356518 tn?1322263642 http://www.iguard.org/r/058JiD8999Cs * * * * WHAT DOES THIS MEAN? This recall for Ultram ER Extended-Release Tablets, 100 mg 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 Ultram ER Extended-Release Tablets, 100 mg, you should follow up with your physician if you are concerned or are experiencing side effects..
874521 tn?1424116797 //efoodalert.blogspot.com/2010/08/fda-focus-on-pet-products-stimulates.
94902 tn?1330479667 There has been a recall of certain Infants and Childrens Tylenol. You can get more info at the following link: www . tylenol.com/page.jhtml?id=tylenol/news/subpchildinfantnews. inc (take out the spaces). Also there is even more info at McNeil Consumer Healthcare that states that the Tylenol may have been exposed Burkholderia cepacia (B. cepacia) bacteria.
Avatar f tn t improved at all in the 6 months he has been seeing me, HOWEVER I am able to control my diplopia about 95% of the time. Currently I will be seen every 3 months to determine if muscle surgery will be performed. In the meantime, I will live with the double vision. My question for you Dr. Hagan, is that if in the future, you do more research on cataract surgery anesthesia and diplopia if I could be involved in your study.
179856 tn?1333547362 The contaminated product has the potential to cause serious problems, including dangerous blood clots, Amgen said in a press release announcing the recall. However, Amgen said there had been no complaints that can be directly attributed to the presence of glass. It said certain lots were being voluntarily recalled as a precaution.
1118724 tn?1357010591 Genentech Informs Customers of Important Information about Triad Group's Alcohol Prep Pads Consumers Alerted to Discontinue Use of Alcohol Prep Pads Packaged with Boniva Injection, Fuzeon, Nutropin A.Q. Pen, Pegasys, TNKase Medicines South San Francisco, Calif. -- January 13, 2011 -- Genentech, Inc.
Avatar n tn Also recently there was a recall on the fentanyl patch for releasing too much of the med too quickly and causing breathing problems among other things.
29837 tn?1414534648 Today I got not one but two calls from the FDA, so apparently my persistence is paying off. They are going to do whatever the pharmaceutical companies suggest, especially since there are no other alternative drugs except Interferon and Ribavirin. My contact at Vertex, who I just spoke to, is going to look once more into the IND application (Compassionate Use), and see if there's been any changes in their (Vertex) policy for allowing it.
675347 tn?1365460645 December 30, 2020 — The FDA is alerting consumers that Midwestern Pet Foods, Inc. is recalling nine lots of Sportmix pet food products because they contain potentially fatal levels of aflatoxin. FDA is aware of at least 28 deaths and 8 illnesses in dogs that ate the recalled products. For more information please go to the website Dog Food Advisor: https://www.dogfoodadvisor.
572651 tn?1530999357 Wow. This is so weird. I only just heard about the recall because I'm on the FDA recall email list. FYI: I'm not paranoid, I'm just on the recall email list because I used to work in the product safety field and I needed to know that type of information. =) Anyway, that recall notice didn't say anything about Copaxone (which is what I'm on), and Shared Solutions hasn't called me or left me any kind of message or sent a letter. That's irritating.
233616 tn?1312787196 According to the company’s recall notice, the action is necessary because cracks in the necks of a small number of Procrit vials were discovered upon post-manufacturing inspection. The Procrit recall involves approximately 44,292 vials of lot P114942A distributed between April 15, 2008 and July 17, 2008.