Angiodynamics recalls BioFlo Midline Convenience Kits containing BD PosiFlush SF Saline Flush Syringes from April 2020 due to BD's recall. 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 Convenience 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 pulled to prevent potential issues with the syringes.
The recall is triggered because BD Medical previously recalled their PosiFlush SF Saline Flush Syringes on April 16, 2020. Angiodynamics is now recalling the kits that contain these syringes to ensure safety, as the syringes may have issues that could affect medical procedures.
Healthcare professionals using these kits for percutaneous introduction of medical devices like catheters or pacing leads are most at risk. Patients receiving care with these kits could be affected if the syringes are used.
Check for item numbers starting with H96560M or PKM followed by specific numbers listed in the recall notice. The kits were sold with specific lots from April 2020, but the exact dates are not provided in the record.
Look for item numbers or lot numbers listed in the recall notice to confirm if your kit is affected.
The BioFlo Midline Convenience Kits contain BD PosiFlush SF Saline Flush Syringes that were recalled by BD Medical on April 16, 2020.
The recall notice does not specify a remedy, so check the item numbers or lot numbers listed to determine if your kit is affected.
Yes, specific item numbers and lots are listed in the recall notice, but the exact dates of sale are not provided.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2396-2020 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2396-2020 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.
