Medtronic recalls SynchroMed II Model 8637 and SynchroMed III Model 8667 pumps used with PROG CT900C Clinician Tablet UK due to software issues in version 2.x. Affected units require software update to prevent potential malfunctions.
Software issues were identified in application version 2.x.
Medtronic is recalling specific implantable nerve stimulation pumps that use a particular clinician tablet app version. The software issue could cause the device to malfunction, potentially affecting patient safety.
The software issues in application version 2.x could cause the device to malfunction. This might lead to improper treatment delivery or unexpected device behavior, though the exact risk level is not specified in the recall notice.
Patients using SynchroMed II Model 8637 or SynchroMed III Model 8667 pumps with the PROG CT900C Clinician Tablet UK and the A810 CP app version 2.x are affected. Healthcare providers who use these devices are most at risk of potential malfunctions.
Check if your device has the SynchroMed II Model 8637 or SynchroMed III Model 8667 pump with the PROG CT900C Clinician Tablet UK and the A810 CP app version 2.x. Serial numbers listed in the recall include NPL1000442 through NPL1002309.
Verify your device's software version by checking the app version on the PROG CT900C Clinician Tablet UK.
Contact Medtronic to update to a newer software version that resolves the identified issues.
No, the recall does not require immediate discontinuation. The software issue can be resolved with an update.
SynchroMed II Model 8637 and SynchroMed III Model 8667 pumps used with PROG CT900C Clinician Tablet UK and A810 CP app version 2.x.
Check the serial numbers listed in the recall notice, which include NPL1000442 through NPL1002309.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0772-2025 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0772-2025 from Medtronic. 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.
