Creganna Medical Devices recalls Gore Tips Set Device (TSET1016) due to possible incorrect expiration dates. Affected lots may need replacement to ensure safe medical use.
Three lots of product may be labeled with an incorrect expiration day
Creg: Creganna Medical Devices is recalling a Gore Tips Set Device (catalog number TSET1016) because some units may have incorrect expiration dates. This could lead to unsafe medical use if the device is used after its actual expiration date.
The device may have an incorrect expiration date, which could lead to unsafe medical use if the device is used after its actual expiration date. This risk is specific to medical procedures requiring precise timing.
Medical professionals using the Gore Tips Set Device for percutaneous liver access are likely affected. Patients receiving this device may be at risk if the expiration date is incorrect.
Check for the catalog number TSET1016 on the device. Affected lots include 1V00099635, 1V00166928, and 1V00199622. The device is used for percutaneous liver access procedures.
Verify the expiration date on the device label to ensure it matches the correct date for safe medical use.
The catalog number is TSET1016.
Affected lots are 1V00099635, 1V00166928, and 1V00199622.
Look for the catalog number TSET1016 and check if your lot number matches 1V00099635, 1V00166928, or 1V00199622.
We’ve drafted a message you can send Creganna Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-2249-2023 — Creganna Medical Devices Creganna Medical Devices Hello, I own a Creganna Medical Devices that is covered by recall Z-2249-2023 from Creganna Medical Devices. 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.
