CLASS II · ModerateFDA

Medtronic Navigation, Inc. recalls Medtronic NDI Passive Spheres REF: 8801075

📅 Aug 31, 2026 · 📍 AK, AL, AR, AZ, CA, CO, CT, DC +44

Recalling company: Medtronic Navigation, Inc.
Product: Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly
Reason: Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
Classification: Class II – may cause temporary or medically reversible health consequences
Recall date: Aug 31, 2026
Reported: Oct 28, 2026
Distribution: US: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA PR RI SC SD TN TX UT VA VT WA WI WV WY OUS: Canary Islands, Iceland, Northern Ireland, Martinique, China , Taiwan, Hong Kong,
Status: Ongoing
Quantity: 476,256 units
Lot / codes: UDI: 00643169278028/ Lots: 2503291 2503331 2503381 2504011 2504021 2504151 2504361 2505101 2505111 2505231 2505291 2505411 2505491 2505661 2506101 2506181 2506401 2506431 2506491 2506501 2509551 2509561 2509831 2510011 2510031 2510171 2510181 2510221 2510241 2510561 2510611 2510771 2510781 2511261 2511521 2511621 2511631 2512091; UDI: 20805832070030/ Lots: 2502431 2512091 2502431 2502461 2502511 2502531 2502541 2503071 2503081 2503091 2503101 2503111 2503121 2503161 2503171 2503181 2503191 2503201 2503211 2503221 2503251 2503261 2503271 2503281 2503291 2503331 2503341 2503351 2503361 2503381 2503401 2504011 2504021 2504041 2504051 2504071 2504101 2504151 2504201 2504281 2504341 2504351 2504361 2504371 2505101 2505111 2505121 2505141 2505161 2505231 2505241 2505251 2505261 2505281 2505291 2505301 2505311 2505361 2505401 2505411 2505491 2505501 2505511 2505601 2505621 2505631 2505661 2506091 2506101 2506111 2506121 2506141 2506151 2506171 2506181 2506191 2506201 2506211 2506261 2506271 2506281 2506351 2506361 2506381 2506401 2506421 2506431 2506461 2506471 2506481 2506491 2506501 2506521 2506531 2506591 2506641 2507081 2507091 2509421 2509431 2509531 2509551 2509561 2509581 2509591 2509601 2509611 2509731 2509741 2509751 2509761 2509771 2509821 2509831 2509841 2510011 2510021 2510031 2510041 2510051 2510061 2510071 2510081 2510091 2510101 2510131 2510141 2510151 2510171 2510181 2510191 2510221 2510231 2510241 2510291 2510531 2510541 2510561 2510571 2510611 2510761 2510771 2510
Company location: Lafayette, CO
Recall type: Voluntary: Firm initiated
Recall number: Z-0196-2027
Agency: U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0196-2027 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.