Cordis recalls one lot of POWERFLEX P3 PTA Dilation Catheter (REF 420-6020S) due to potential body shaft voids in the proximal seal area. Affected units have lot number 82155955 with use by date 2021-06-30.
Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft voids in the proximal seal area.
Cordis is recalling a specific lot of POWERFLEX P3 PTA Dilation Catheter because it may have body shaft voids in the proximal seal area. This could lead to improper sealing during medical procedures, potentially causing complications.
The catheter may have voids in the proximal seal area, which could allow fluid or tissue to leak during medical procedures. This might cause improper sealing and potentially lead to complications like infections or ineffective treatment.
Medical professionals using the Cordis POWERFLEX P3 PTA Dilation Catheter for procedures are likely affected. Patients undergoing procedures with this specific lot may be at risk.
Check for the lot number 82155955 on the catheter packaging. The use by date for this lot is June 30, 2021. This specific lot was sold by Cordis Corporation.
Look for the lot number 82155955 on the catheter packaging or label.
The recall states there is a potential for body shaft voids in the proximal seal area, which could lead to complications during medical procedures. However, the exact risk level is not specified in the recall notice.
The recall does not provide specific action steps for users. You should check the lot number to see if your catheter is affected.
Check the lot number 82155955 on the catheter packaging. The use by date for this lot is June 30, 2021.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-1477-2020 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-1477-2020 from Cordis. 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.
