Cordis recalls specific lots of PRECISE PRO RX carotid stent implants due to risk of distal tip separation from lumen wire. Affected product codes and lot numbers listed.
Distal tip may become separated from the lumen wire in specific lots.
Cordis is recalling certain lots of PRECISE PRO RX carotid stent implants because the distal tip may separate from the lumen wire in specific batches. This could lead to improper placement or complications during medical procedures.
The distal tip of the stent may become separated from the lumen wire in specific batches, potentially causing improper placement during medical procedures. This could lead to complications if the stent does not function correctly.
Patients who received the recalled carotid stent implants during surgery are likely affected. Medical professionals using these implants for procedures are at risk if they handle the affected lots.
Check the product code (PC0520RXC through PC1040RXC) and lot number listed in the recall notice. The affected lots are detailed in the product codes and specific lot numbers provided.
Review the product code and lot number on your implant to see if it matches the recalled items listed in the notice.
Cordis is recalling specific lots of PRECISE PRO RX carotid stent implants with product codes PC0520RXC through PC1040RXC.
Check the product code and lot number on your implant against the list of affected codes and lot numbers provided in the recall notice.
The recall does not specify a remedy, so no action is required unless your implant matches the affected product codes and lot numbers.
We’ve drafted a message you can send Cordis to request your refund or repair — edit it as you like.
Subject: Recall Z-1257-2021 — Cordis Cordis Hello, I own a Cordis that is covered by recall Z-1257-2021 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.
