digitek recall 2008

00 -0500 Actavis Totowa LLC, a United States manufacturing division of the international generic pharmaceutical company Actavis Group, is initiating a Class I nationwide recall of Digitek (digoxin tablets, USP, all strengths) for oral use. The products are distributed by Mylan Pharmaceuticals Inc., under a "Bertek" label and by UDL Laboratories, Inc. under a "UDL" label.

I was talking to my husband just the other day about her. We were speaking about the old digoxin recall (back in April) that was posted and I was wondering how she was doing. I'm so glad to hear the good news. Now hopefully the pac's will ease up too. :-) Take care.

For those on Heparin: my RE's office told me there has been a recall on Heparin manufactured by Baxter. Here's some more information: http://www.baxter.com/about_baxter/news_room/news_releases/2008/02-28-08-heparin.html check with your Dr.

I did have a chest infection about one-month before my last heart episode. Did you also hear about the Digitek recall and that problem? I stopped taking it the week my breathing problem stopped?

I did have a chest infection about one-month before my last heart episode. Did you also hear about the Digitek recall and that problem? I stopped taking it the week my breathing problem stopped?

Lanoxin has not been recalled.... digitek was recalled..

As Toprol also reduces blood pressure and I have low blood pressure as it is, I started having dizziness and nausea. He then put me on Digitek, which has since been recalled and I havebeen on 0.25 mg of digoxin for about 2 months. I recently started to have cramps, abnormal bowel movements and I feel very exhausted. The doctor reduced the dosage to .125 mg and on the first day I felt better until about 6PM and then the cramps started again.

Recall Alert! About 800,000 Dorel car seats have been recalled. http://bit.

The Procrit recall involves approximately 44,292 vials of lot P114942A distributed between April 15, 2008 and July 17, 2008.

Fri, Sep 19, 2008 (BabyCenter News) — Simplicity has announced a recall of about 600,000 drop-side cribs in cooperation with the Consumer Product Safety Commission (CPSC). Due to sizing problems with the crib's hardware, the drop side — the side of the crib that lowers — can come off the tracks, creating a hazardous gap. If this happens, a child could get caught in the gap and suffocate.

This is my story on 27th may 2008 I mixed up foods during breakfast and throughout the day until launch then I threw up ....Since that day I have been in constant nausea/ vomiting for about 2 weeks then things settled down.But one thing was weird to me I had excess salivation ever since that day(27th may 2008) onwards(till today) after any meal I would have so much silva that I just have to go to the bathroom every 5mins to release it.

I've been treated for syphilis last 2008. this 2012 i decided to go abroad and i passed the interview then proceed to medical, unfortunately i've been traced to be tpha positive, what am i going to do next.?

Hi, I have this question because recently I need to take a blood test and I haven't done that for more than 12 years. I always had protected sex but I didn't have an partner after 2008. Back in 2007, or 2008, I fingered my partner and I don't remember if I had any cuts or not. I don't recall to have any flu or swollen lymph after that and I have been completely normal since.

http://www.fda.gov/foi/warning_letters/s6760c.htm I've done my best to become informed on hip replacements, e.g. the choices of materials and methods used and have discussed these things with my surgeon to come up with the best plan for me. But in the process I also learned about the recalls, the deals manufacturers have made with surgeons, the AAOS letter to help cover it, etc. I am scheduled for hip replacement surgery soon.

More than 985,000 previously recalled drop-side cribs have been recalled again to repair missing safety pegs that create a risk of entrapment and suffocation. Recall Reason Many styles of crib are included in this recall. Image here represents just one. The US Consumer Product Safety Commission (CPSC) and Delta Enterprise Corp., of New York, New York, are re-announcing the 2008 recall of more than 985,000 drop-side cribs with "Crib Trigger Lock and Safety Peg" hardware.

I have been following these forums for a few months but want to post this question any way. From 2007 to 2008 i have had several sexual encounters. Most of them have been with CSW and have been condom protected for both oral and vaginal intercourse. At no time do i recall the condom breaking or slippage. However i have both received and performed unprotected oral sex on 3 males of unknown status from march 2007 to April 2007.

Why was c-phen dm infant drops recalled?

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.

The Food and Drug Administration reported more than 1,742 recalls last year, skyrocketing from 426 in 2008, according to the Gold Sheet, a trade publication on drug quality that analyzes FDA data. 2092 diggs diggEmail Print CommentOne company, drug repackager Advantage Dose, accounted for more than 1,000 of those recalls. Even excluding Advantage Dose, which has shut down, recalls jumped 50% last year.

I would go by the due date based on the sonogram. Doctor's use a mathematican equation based on your LMP to determine your due date. If you do not give them an accurate LMP then of course his due date is wrong. Go by what the sonogram said.

Digitek recall 2008

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