Reported Oct 28, 2026 · Ongoing · Updated Nov 2, 2026
InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030
Medtronic Neuromodulation
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 Neuromodulation · 7000 Central Ave Ne · Minneapolis, MN · 55432-3568
Is this the product you have?
- InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT 3560030 ISTM MICRO PERC 3560030
- Lot codes and dates
- 3560022 UDI-DI 00763000203894 LotsUDI-DI 00763000587062 Lots
2,169 of 2,169 codes
VA24HE7VA24R5JVA24TXTVA24UYBVA24WJEVA24WJFVA250XHVA25144VA2515AVA25TEFVA25TEHVA25TEJVA25TELVA26A7FVA26AJAVA26AJBVA26AKSVA26AKTVA26AKUVA26AKVVA26C4TVA26CB1VA26CB2VA26EHLVA26EHNVA26EHPVA2725RVA2725SVA2726HVA2726JVA2728HVA2728KVA2728LVA275QEVA2760FVA277W0VA277W1VA27C85VA27C86VA27CCGVA27CEEVA27D4BVA27D62VA27D63VA27KEHVA27KGXVA27KHGVA27KHHVA27KHJVA27KHKVA27KHLVA27NS0VA27NSCVA27NSGVA27NSHVA27NSJVA27NSLVA27ST1VA27ST2VA27UGK
VA3A3MU; 3560030 UDI-DI 00763000203887 LotsVA2JLZTVA2JMYGVA2JQGQVA2NCB1VA2NN7RVA2NN95VA2NN9VVA2P2N4VA2P9VMVA2PA8WVA2PCP0VA2S1KDVA2S1KFVA2S1V2VA2SCUYVA30ZT4VA31KGBVA31LNSVA31LNVVA31LP1VA31LP4VA31MZBVA31SVZVA31VE9VA321PUVA322AMVA322DDVA34D3ZVA34K6DVA34P48VA34U6MVA34U9HVA350N9VA35509VA356M3VA35JLYVA35JMLVA36Z5HVA376T5VA37KGKVA37P5GVA37TVWVA383BPVA3848VVA38GHXVA38N4PVA38YL3VA3A22U
UDI-DI 00763000587000 Lots257 of 257 codes
VA24HE0VA24Q0FVA24QEDVA24QEFVA24WJDVA25181VA25182VA26CMDVA26CMZVA26CN0VA26CN1VA26CN3VA26E7AVA26EGFVA26EGGVA275QFVA275QGVA2760GVA276AWVA276AXVA276GMVA276GNVA276GPVA277MVVA277PRVA277V8VA277V9VA277VUVA277VVVA277VWVA27CCUVA27CGBVA27CGCVA27CGDVA27D43VA27D44VA27D5WVA27UGHVA27UW3VA27YHAVA27YKPVA280D2VA280MVVA28488VA2871DVA2872XVA28BHFVA28BHGVA28BLLVA28BQ1VA28BR1VA28BR2VA28K4UVA28Z67VA28Z6BVA28Z6NVA28Z6PVA28Z6XVA28Z9MVA29ES2
VA2F0R7VA2GT10VA2LH1ZVA2M7F8VA2QET4VA2QEUEVA2T1HAVA2TSXSVA2TSYMVA2VKJMVA2WPMQVA2WPMSVA2YVJAVA2Z4UGVA334P0
- 3560022 UDI-DI 00763000203894 Lots
- Amount recalled
- 56,331 (US); 40,211 (OUS)
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may result in delay of surgery or need for surgical replacement of the product.
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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