Bard recalls X-Port MRI implantable ports with specific catheter models due to risk of incorrect catheter tip causing prolonged surgery. Affected units have unique reference numbers and lots.
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 two specific models of MRI-compatible implantable ports that may have the wrong catheter tip. This could lead to longer surgical procedures if the port is used incorrectly.
The port may contain a tunneler with a barb tip designed for a smaller catheter (6Fr) instead of the correct larger catheter (9.6Fr). This mismatch can cause the procedure to take longer than intended during surgery.
Patients using Bard X-Port MRI implantable ports with the specified reference numbers and lots are affected. Medical professionals who have these ports in their patient care are most at risk.
Check for reference numbers REF:0607550 or REF:0657525 on the product packaging. The lot numbers RECR1508 or RECU1597 are also associated with these models.
Look for reference numbers REF:0607550 or REF:0657525 and lot numbers RECR1508 or RECU1597 on the product packaging.
Bard identified that the product may contain a tunneler with a barb tip meant for a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter, which could prolong surgery.
The official recall notice does not specify a remedy, so check with Bard directly for guidance.
Yes, the affected units have lot numbers RECR1508 (REF:0607550) and RECU1597 (REF:0657525).
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1578-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1578-2020 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.
