Bard recalls specific implantable ports that may contain incorrect catheter tips, potentially prolonging surgery. Affected units include those with reference number 0604550 and lot number RECR1431.
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 implantable ports that might have the wrong catheter tip, which could lead to longer surgeries. This is a safety issue for patients needing repeated vascular access.
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, potentially delaying critical medical care.
Patients using BardPort M.R.I. Hard Base Implantable Ports with reference number 0604550 and lot number RECR1431 are most at risk. Healthcare providers who use these ports for medical treatments may also be affected.
Check for the reference number 0604550 and lot number RECR1431 on the product label. The product is used for medical treatments requiring repeated vascular access.
Look for the reference number 0604550 and lot number RECR1431 on the product label.
The recalled model is BardPort M.R.I. Hard Base Implantable Port with reference number 0604550.
The product may contain a tunneler with a barb tip meant for a 6Fr catheter instead of the correct 9.6Fr catheter, which can prolong surgery.
Check for the reference number 0604550 and lot number RECR1431 on the product label.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1577-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1577-2020 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.
