Angiodynamics recalls BioFlo and Xcela PICC Convenience Kits that contain BD PosiFlush SF Saline Flush Syringes, which were previously recalled by BD Medical on April 16, 2020.
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 Convenience Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical on April 16, 2020. These kits are used for intravenous therapy, blood sampling, and administering medications. The recall affects specific model numbers and lots listed in the notice.
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 described in the notice, so the risk level cannot be determined.
Healthcare professionals and patients using intravenous therapy who own the recalled BioFlo or Xcela PICC kits are affected. Those with the specific model numbers and lots listed in the recall notice are most at risk.
Check for the model numbers and lots listed in the recall notice. The kits contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical on April 16, 2020.
Review the model numbers and lots listed in the recall notice to confirm if your kit is affected.
The BioFlo and Xcela PICC kits contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical on April 16, 2020.
Check the model numbers and lots listed in the recall notice to see if your kit is affected. If it is, you should contact Angiodynamics for further instructions.
The recall notice does not specify the hazard mechanism, so the risk level cannot be determined.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2397-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2397-2020 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.
