Bolton Medical recalls RELAY PRO Thoracic Stent-Graft System (REF 28-N4-XX-XXX-XXX) with UDIUDI/DI numbers listed. Product may be shorter than packaging indicates. Check lot numbers for affected units.
The product may be shorter than packaging indicates
Bolton Medical is recalling their RELAY PRO Thoracic Stent-Graft System because it may be shorter than what's shown on the packaging. This could cause issues during medical procedures if the device doesn't fit properly. Affected units have specific lot numbers listed in the recall.
The product may be shorter than the packaging indicates, which could lead to improper fitting during medical procedures. This might cause complications if the device doesn't align correctly with the patient's anatomy.
Patients who have received the RELAY PRO Thoracic Stent-Graft System with the listed lot numbers are most at risk. Healthcare providers using this device for procedures may also need to check if their equipment is affected.
Check the UDIUDI/DI number on the device packaging or label. Affected units have specific lot numbers listed in the recall, including combinations like B210719245, B220323028, and others as detailed in the official notice.
Look for the UDIUDI/DI number on the device packaging or label to identify if it matches the listed lot numbers in the recall.
The product may be shorter than packaging indicates, but it is not unsafe to use if it matches the correct lot numbers. Affected units should be checked for recall.
Check the UDIUDI/DI number on your device packaging or label. If it matches the listed lot numbers in the recall, it is affected.
Contact Bolton Medical directly to confirm if your device is affected and follow their instructions for next steps.
We’ve drafted a message you can send Bolton Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0998-2023 — Bolton Medical Bolton Medical Hello, I own a Bolton Medical that is covered by recall Z-0998-2023 from Bolton Medical. 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.
