Angiodynamics recalls BioFlo Midline Catheter and Maximal Barrier Kits containing BD PosiFlush SF Saline Flush Syringes, which were recalled by BD Medical on April 16, 2020. Affected units 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 Midline Catheter and BioFlo Maximal Barrier Kits that contain BD PosiFlush SF Saline Flush Syringes. These syringes were previously recalled by BD Medical on April 16, 2020, so the kits are being recalled as part of that action.
The recall involves BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical on April 16, 2020. The specific hazard mechanism isn't clearly described in the notice, so the risk level cannot be determined.
Healthcare professionals using these kits for medical procedures are likely affected. Patients receiving care with these kits may be at risk if they have been exposed to the recalled items.
Check for item numbers starting with H965460 or Cat. No. 46-015 to 46-490. Also look for lots listed in the detailed list provided in the recall notice.
Review the item numbers and lots listed in the recall notice to confirm if your kit is affected.
The BioFlo kits contain BD PosiFlush SF Saline Flush Syringes that were recalled by BD Medical on April 16, 2020. Angiodynamics is recalling these kits as part of that action.
The recall notice does not specify a remedy or action steps for affected users.
Yes, the recall includes specific item numbers (H965460151 to H965464901) and lots listed in the detailed list provided in the notice.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2395-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2395-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
