In the agency's Nov 18, 2026 enforcement report · Ongoing
PROGRAMMER 24970A, provides the analyzer and ECG hardware during device implant, invasive troubleshooting, and…
Medtronic, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic, Inc. · 8200 Coral Sea St Ne · Mounds View, MN · 55112-4391
Is this the product you have?
- PROGRAMMER 24970A, provides the analyzer and ECG hardware during device implant, invasive troubleshooting, and implanted device follow-up procedures, Product Number 24970A
- Lot codes and dates
- UDI-DI
0076300004468800643169957657007630002013330076300020128900763000201296007630002039790076300028805100763000203962007630003177820076300031776800763000397821007630004243430076300042429900763000518981007630005189670076300068840000763000688455007630006884620076300082541600763000688424007630008502340076300085024100763000688448007630008762650076300087627200763000967192
- Serial NumbersSPM
5,888 of 5,888 codes
SPM001252ASPM001274ASPM001303ASPM001309ASPM001317ASPM001321ASPM001323ASPM001332ASPM001375ASPM001505ASPM001554ASPM001565ASPM001576ASPM001582ASPM001585ASPM001588ASPM001589ASPM001611ASPM001619ASPM001624ASPM001634ASPM001645ASPM001657ASPM001660ASPM001673ASPM001686ASPM001687ASPM001690ASPM001698ASPM001712ASPM001713ASPM001753ASPM001769ASPM001793ASPM001812ASPM001820ASPM001972ASPM001978ASPM001989ASPM001995ASPM002001ASPM002002ASPM002003ASPM002004ASPM002006ASPM002009ASPM002011ASPM002012ASPM002013ASPM002014ASPM002015ASPM002067ASPM002088ASPM002092ASPM002097ASPM002106ASPM002107ASPM002111ASPM002112ASPM002115A
5,414 of 5,414 codes
009579ASPM009581ASPM009582ASPM009583ASPM009584ASPM009585ASPM009586ASPM009587ASPM009589ASPM009590ASPM009591ASPM009594ASPM009595ASPM009599ASPM009600ASPM009603ASPM009604ASPM009606ASPM009608ASPM009609ASPM009610ASPM009611ASPM009613ASPM009614ASPM009615ASPM009616ASPM009618ASPM009622ASPM009623ASPM009624ASPM009625ASPM009626ASPM009627ASPM009628ASPM009635ASPM009636ASPM009637ASPM009639ASPM009641ASPM009642ASPM009644ASPM009646ASPM009648ASPM009650ASPM009653ASPM009657ASPM009658ASPM009659ASPM009661ASPM009662ASPM009665ASPM009668ASPM009670ASPM009671ASPM009674ASPM009675ASPM009677ASPM009678ASPM009679ASPM009680A
- UDI-DI
- Amount recalled
- 11301 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Bluetooth disconnections may occur between the device manager software and its associated accessories. Bluetooth disconnections during a SmartSync patient session may lead to harm due to undesirable or incomplete parameter programming.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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