Bard recalls PowerPort MRI implantable ports with potential incorrect catheter attachment causing prolonged surgery. Affected models include specific reference numbers and lot codes. 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 certain PowerPort MRI implantable ports that may have incorrect catheter attachments. This could lead to longer surgical procedures if the port is used improperly.
The product may contain a tunneler with a barb tip designed for a smaller catheter (6Fr) instead of the correct size (9.6Fr). This mismatch can cause the catheter to become stuck during surgery, prolonging the procedure.
Patients receiving vascular access treatments using the recalled PowerPort MRI ports are at risk. Medical professionals who use these ports for infusion therapy or blood sampling may need to check compatibility.
Check for model numbers 1809660, 1809661, 1859660, or 1859661 on the product label. The recall includes specific lot numbers like RECT0092, RECT0190, and others listed in the product description.
Look for model numbers 1809660, 1809661, 1859660, or 1859661 on the product label.
Reach out to Bard Peripheral Vascular Inc for specific guidance on the recall and potential remedies.
The product may contain a tunneler with a barb tip meant for a 6Fr catheter instead of the correct 9.6Fr catheter, which can cause prolonged surgery.
Models with reference numbers 1809660, 1809661, 1859660, and 1859661 are affected, along with specific lot numbers listed in the product description.
No immediate stop is required, but patients and medical professionals should check the product label and contact Bard for guidance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1572-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1572-2020 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.
