Bard recalls PowerPort M.R.I. Implantable Ports with 9.6F catheters that may contain incorrect barb tips, potentially prolonging surgery. Affected units have specific reference numbers and lot numbers.
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 M.R.I. Implantable Ports with 9.6F catheters that may have the wrong type of barb tip. This could cause surgery to last longer than necessary, which is a serious risk for patients needing repeated medical access.
The recalled ports 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 catheter to become stuck during surgery, leading to longer procedures and potential complications.
Patients with Bard PowerPort M.R.I. Implantable Ports using the recalled catheters are most at risk. Healthcare providers who use these devices for medical treatments may also be affected.
Check for reference numbers: 1809600, 1809601, or 1859600. The product includes specific lot numbers like RECR1434, RECT0091, or RECR2072. These units were sold with the described catheter types.
Look for reference numbers 1809600, 1809601, or 1859600 on the device packaging or label.
If you have the recalled device, contact your healthcare provider to discuss potential risks and next steps.
The recalled ports 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 can prolong surgery.
Check for reference numbers 1809600, 1809601, or 1859600 on the device packaging or label, and lot numbers like RECR1434, RECT0091, or RECR2072.
No, but you should contact your healthcare provider to discuss potential risks and next steps.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1571-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1571-2020 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.
