BioFlo Midline Convenience Kits - Product Usage: These recall
BioFlo Midline Convenience Kits - Product Usage: These introducers are used for the percutaneous introduction of diagnostic or therapeutic devices…
Why was BioFlo Midline Convenience Kits - Product Usage: These recalled?
Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lots 5513075 5543988 5569542 5580342* 5488819 5513069 5555125 5569548 5454444 5469653 5503014 5505722 5463227 5468512 5480502 5502087 5519226 5530266 5546401 5552137 5569550 5488815 5580584* 5474463 5513067 5571888 5462690 5472106 5502077 5513079 5528683 5546415 5557545 5566356 5488825 5530192 5576297* 5580586* 5588914* 5468514 5478046 5491839 5496906 5500243 5536950 5574449 5587258 5564674 5470097 5470834 5477983 5482399 5532402 5536956 5567559 5571900 5578553 5543994 5588900* 5574116 5477356 5479479 5492926 5497561 5542304 5550981 5504522 5542305 5584024 5584039 5470195 5472104 5477938 5505005 5523169 5528676 5534740 5539980 5498245 5564682 5571896* 5580582* 5587276* 5468492 5470191 5472098 5488811 5505003 5532394 5536962 5557555 5567546 5587263* 5501851 5501853 5470197 5480508 5500249 5504999 5523173 5546417 5566339 5530185 5519216 5523155 5526006 5536958 5559207 5585529* 5587815* 5560886 5513081 5539976 5589180* 5557537 5548425 5505070 5481670 5486489 5536936 5504526 5504527 5477373 5586746 *All units of these lots are within AngioDynamics control (US and OUS Inventory) and not distributed, therefore, removed from recall notification.
- Product
- BioFlo Midline Convenience Kits - Product Usage: These introducers are used for the percutaneous introduction of diagnostic or therapeutic devices…
- Recalling firm
- Angiodynamics, Inc.
- Quantity
- 119723 eaches total
- Distribution
- US Nationwide distribution.
- Recall date
- June 24, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)