In the agency's Nov 18, 2026 enforcement report · Ongoing
RF HEAD 24967 PATIENT CONNECTOR and RF HEAD 24967 EUR MKT, communicates with Medtronic cardiac devices, Product Number…
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?
- RF HEAD 24967 PATIENT CONNECTOR and RF HEAD 24967 EUR MKT, communicates with Medtronic cardiac devices, Product Number 24967
- Lot codes and dates
- UDI-DI
0076300006043500763000060428007630000604420076300006045900763000288242007630002575830076300025761300763000317799007630002575760076300031777500763000208394007630004243740076300068847900763000688509007630006885160076300068853000763000688554007630006884930076300068854700763000688486
- Serial Numbers
11,743 of 11,743 codes
RFA001598ARFA001602ARFA001786ARFA001826ARFA002016ARFA002095ARFA002591ARFA003113ARFA003146ARFA003306ARFA005031ARFA005097ARFA005103ARFA008830ARFA014171ARFA014218ARFA014252ARFA014258ARFA014278ARFA014286ARFA014342ARFA014609ARFA014653ARFA014885ARFA014952ARFA014996ARFA015015ARFA016648ARFA016815ARFA016817ARFA017064ARFA017468ARFA017880ARFA017906ARFA017907ARFA017929ARFA017947ARFA018801ARFA019059ARFA021437ARFA021450ARFA021477ARFA021618ARFA021626ARFA021652ARFA021661ARFA036107ARFA036123ARFA036190ARFA036411ARFA036460ARFA037606ARFA037647ARFA037648ARFA037650ARFA037794ARFA038977ARFA039112ARFA039113ARFA040362A
- UDI-DI
- Amount recalled
- 11741 untis
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.
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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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