Medtronic recalls Duet External Drainage and Monitoring system with incorrect expiration date labeling. Affected units may have safety risks due to outdated expiration dates.
Product labeling contains incorrect expiration date
Medtronic is recalling a specific Duet External Drainage and Monitoring system because its labeling has an incorrect expiration date. This could lead to improper use if the product is used after its actual expiration date.
The product's expiration date label is incorrect, which could lead to using the device after it has expired. Expired medical devices may not function properly or could pose safety risks during medical procedures.
Patients using the Medtronic Duet system with the specific lot number and UDI-DI code are affected. Healthcare providers who use this system for medical procedures may also be at risk.
Check for the lot number 226632942 and UDI-DI code 00763000624781 on the product packaging. This system is sold as a sterile, prescription-only device for medical use.
Look for the lot number 226632942 and UDI-DI code 00763000624781 on the product packaging.
The product may be safe if the expiration date label is correct, but the recall indicates an incorrect expiration date label which could lead to improper use.
Check for the lot number 226632942 and UDI-DI code 00763000624781 on the product packaging.
The recall does not specify a remedy, so contact Medtronic for further instructions.
We’ve drafted a message you can send Medtronic Neurosurgery to request your refund or repair — edit it as you like.
Subject: Recall Z-2412-2023 — Medtronic Neurosurgery Medtronic Neurosurgery Hello, I own a Medtronic Neurosurgery that is covered by recall Z-2412-2023 from Medtronic Neurosurgery. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
