amym1586 Posted June 24, 2016 Share Posted June 24, 2016 Anyone else here affected by the blood recall with the defective leukocyte filters ? I think that sums up my week. Link to comment Share on other sites More sharing options...
Malcolm Needs ☆ Posted June 24, 2016 Share Posted June 24, 2016 Oh Dear! Gnapplec and amym1586 2 Link to comment Share on other sites More sharing options...
mollyredone Posted June 24, 2016 Share Posted June 24, 2016 Yes, but all the units that were recalled for us (so far) had already been transfused. Link to comment Share on other sites More sharing options...
amym1586 Posted June 25, 2016 Author Share Posted June 25, 2016 19 hours ago, mollyredone said: Yes, but all the units that were recalled for us (so far) had already been transfused. We had transfused quite a bit of ours too. Is your hospital doing any follow up with patients that got the units? Link to comment Share on other sites More sharing options...
mollyredone Posted June 25, 2016 Share Posted June 25, 2016 Not so far. I haven't heard back from my medical director. I would think it would only affect patients who were at risk for CMV or TA-GVHD. I have also checked my transfusion reactions and haven't encountered one of those units yet. So my feeling is if they haven't had a reaction by now, they probably won't or we would have heard about it. amym1586 1 Link to comment Share on other sites More sharing options...
amym1586 Posted June 26, 2016 Author Share Posted June 26, 2016 I'm the same way. But my MD is very umm.. I can't think of a word. But there's a good chance he'll want me diving in to every patient that got transfused. I feel like our blood supplier also should be telling us how to handle this since the FDA is involved. Link to comment Share on other sites More sharing options...
Maureen Posted June 28, 2016 Share Posted June 28, 2016 The FDA states to report adverse events. We are notifying the ordering providers of transfused patients, with a request to let us know of any unexpected clinical events have occurred subsequently, which could be related to this transfusion. Link to comment Share on other sites More sharing options...
amym1586 Posted June 29, 2016 Author Share Posted June 29, 2016 Some of these units on my list were transfused over a month ago. I'm already up to 100 units and I'm still not finished going through it. My blood supplier has given us ZERO information on what to do. Only to keep a record of it. Link to comment Share on other sites More sharing options...
ESIZENSKY Posted June 29, 2016 Share Posted June 29, 2016 We are now receiving Red Blood Cells non leukoreduced. How is everyone managing RBC transfusions for their patients? We are limiting RBC transfusions for trauma and non oncology patients? Does anyone have a deviation policy to use RBCs? Link to comment Share on other sites More sharing options...
amym1586 Posted June 29, 2016 Author Share Posted June 29, 2016 At first we ordered some Non LR but we don't have an option for doctors to order NonLR RBCs and we don't have any products built in our system to be NonLR and it was going to be a nightmare. So, we called a new blood supplier and they got our shelves filled. Link to comment Share on other sites More sharing options...
David Saikin Posted July 4, 2016 Share Posted July 4, 2016 I just walked into this in my new position . . . WOW. I think we are doing a f/u on all transfusions to determine if the patients were definitive candidates for leukos or not. This is my task starting tomorrow. Waiting for a complete list from the blood supplier. amym1586 1 Link to comment Share on other sites More sharing options...
Eagle Eye Posted July 6, 2016 Share Posted July 6, 2016 Good Luck David! and Congratulation.... Link to comment Share on other sites More sharing options...
amym1586 Posted July 14, 2016 Author Share Posted July 14, 2016 On 7/4/2016 at 0:40 PM, David Saikin said: I just walked into this in my new position . . . WOW. I think we are doing a f/u on all transfusions to determine if the patients were definitive candidates for leukos or not. This is my task starting tomorrow. Waiting for a complete list from the blood supplier. I know you're probably busy. I've called the Doctor employed by our Blood Supplier, I've called the FDA. If I can get a number I'll call Haemonetics. I can't seem to get anything in writing about what the heck we're suppose to be doing. What documentation I need to be doing so this doesn't come back on us. what are you doing? Gnapplec 1 Link to comment Share on other sites More sharing options...
David Saikin Posted July 15, 2016 Share Posted July 15, 2016 17 hours ago, amym1586 said: I know you're probably busy. I've called the Doctor employed by our Blood Supplier, I've called the FDA. If I can get a number I'll call Haemonetics. I can't seem to get anything in writing about what the heck we're suppose to be doing. What documentation I need to be doing so this doesn't come back on us. what are you doing? Still waiting for an excel listing of units - should come today. We are in a bit of a quandary. We are going to see if we transfused units or not . We may just issue a blanket statement to our MDs stating the problem and that if they had patients transfused during the recall period they can contact the BB to see if they rec'd the non-leukos or routine inventory. We have a lot of impacted units. amym1586 1 Link to comment Share on other sites More sharing options...
amym1586 Posted July 15, 2016 Author Share Posted July 15, 2016 2 hours ago, David Saikin said: Still waiting for an excel listing of units - should come today. We are in a bit of a quandary. We are going to see if we transfused units or not . We may just issue a blanket statement to our MDs stating the problem and that if they had patients transfused during the recall period they can contact the BB to see if they rec'd the non-leukos or routine inventory. We have a lot of impacted units. I think I have ~130 last I looked. Blanket statement sounds good. The Doctor on staff with United Blood Services assured me that the FDA was not mandating that we report to clinicians. She said she checked the diagnosis of each patient that received a unit and looked to see if any patients were on a transplant list. She checked for any transfusion reactions. She assured me it was minimal risk of any problems, not much for a doctor to do now and that the units were at least 90-95 % LR. Gnapplec and David Saikin 2 Link to comment Share on other sites More sharing options...
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