Angiodynamics recalls BioFlo and Xcela PICC Maximal Barrier Nursing Kits that contain BD PosiFlush SF Saline Flush Syringes, which were recalled by BD Medical on April 16, 2020. Affected kits include specific item numbers and lots.
Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020.
Angiodynamics is recalling BioFlo and Xcela PICC Maximal Barrier Nursing Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical on April 16, 2020. This recall affects specific product models and lots.
The recall is due to BD PosiFlush SF Saline Flush Syringes being previously recalled by BD Medical on April 16, 2020. However, the specific hazard mechanism is not clearly described in the record.
Healthcare professionals who use these kits for intravenous therapy, particularly those in hospitals or clinics. Patients receiving IV treatments with these kits are at risk if they have the recalled items.
Check for item numbers starting with H965750011 through H965750701 or catalog numbers 75-001 through 75-070. Also, look for specific lots listed in the record, such as 5532456, 5546446, etc.
Review the item numbers and catalog numbers listed in the recall notice to confirm if your kit is affected.
The BioFlo and Xcela PICC Maximal Barrier Nursing Kits contain BD PosiFlush SF Saline Flush Syringes that were recalled by BD Medical on April 16, 2020.
The official recall notice does not specify a remedy or action steps beyond checking product details.
Yes, the recall includes specific item numbers (H965750011 to H965750701) and lots listed in the record, such as 5532456, 5546446, etc.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2398-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2398-2020 from Angiodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
