Bard recalls PowerFlow implantable apheresis ports with 9.6F catheters that may contain wrong catheter tips, causing prolonged procedures. Affected patients should contact Bard for details.
Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
Bard is recalling a specific type of IV port system that may have the wrong catheter tip, which could lead to longer medical procedures. This is a safety issue for patients using the device for treatments.
The port system may include a catheter tip designed for a smaller catheter (6Fr) instead of the correct larger size (9.6Fr). This mismatch can cause the procedure to take longer than intended, potentially delaying treatment.
Patients using Bard PowerFlow implantable apheresis ports with the specific model and lot number are affected. Those with medical conditions requiring frequent IV access are most at risk.
Check for the model number A710962 and lot number RECR1499 on the product label. The product was sold with a specific UDI code (01)00801741129438.
Look for model number A710962 and lot number RECR1499 on the device label.
The product may contain a catheter tip meant for a smaller catheter (6Fr) instead of the correct size (9.6Fr), which can prolong medical procedures.
Contact Bard directly for details about your specific product and next steps.
The recall states a risk of prolonged procedures, but no mention of serious injury or death. The danger level is low risk.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1579-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1579-2020 from Bard. 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.
