CLASS II · ModerateFDA

Medtronic, Inc. recalls CareLink SmartSync Programmer

📅 Sep 24, 2026 · 📍 See notice

Recalling company: Medtronic, Inc.
Product: CareLink SmartSync Programmer, Model 24970A, Pulse generator, permanent, implantable
Reason: Software problem has the potential for an inaccurate displayed longevity estimate.
Classification: Class II – may cause temporary or medically reversible health consequences
Recall date: Sep 24, 2026
Reported: Nov 4, 2026
Distribution: Worldwide distribution.
Status: Ongoing
Quantity: 11238 units
Lot / codes: GTIN 00763000044688, Serial Number SPM001252A; GTIN 00763000044688, Serial Number SPM001274A; GTIN 00763000044688, Serial Number SPM001303A; GTIN 00763000044688, Serial Number SPM001309A; GTIN 00763000044688, Serial Number SPM001317A; GTIN 00763000044688, Serial Number SPM001321A; GTIN 00763000044688, Serial Number SPM001323A; GTIN 00763000044688, Serial Number SPM001332A; GTIN 00763000044688, Serial Number SPM001375A; GTIN 00763000044688, Serial Number SPM001505A; GTIN 00763000044688, Serial Number SPM001554A; GTIN 00763000044688, Serial Number SPM001565A; GTIN 00763000044688, Serial Number SPM001576A; GTIN 00763000044688, Serial Number SPM001582A; GTIN 00763000044688, Serial Number SPM001585A; GTIN 00763000044688, Serial Number SPM001588A; GTIN 00763000044688, Serial Number SPM001589A; GTIN 00763000044688, Serial Number SPM001611A; GTIN 00763000044688, Serial Number SPM001619A; GTIN 00763000044688, Serial Number SPM001624A; GTIN 00763000044688, Serial Number SPM001634A; GTIN 00763000044688, Serial Number SPM001645A; GTIN 00763000044688, Serial Number SPM001657A; GTIN 00763000044688, Serial Number SPM001660A; GTIN 00763000044688, Serial Number SPM001673A; GTIN 00763000044688, Serial Number SPM001686A; GTIN 00763000044688, Serial Number SPM001687A; GTIN 00763000044688, Serial Number SPM001690A; GTIN 00763000044688, Serial Number SPM001698A; GTIN 00763000044688, Serial Number SPM001712A; GTIN 00763000044688, Serial Number SPM001713A; GTIN 0076300
Company location: Mounds View, MN
Recall type: Voluntary: Firm initiated
Recall number: Z-0302-2027
Agency: U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0302-2027 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.