Data Foundry

Medical device recalls 2025

SmartPath to dStream for XR and 3 — Class II medical device recall Z-2216-2025

Ongoing recall by Philips North America, reported 2025-08-06, distributed nationwide. The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source

Recall numberZ-2216-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmPhilips North America, Cambridge, MA, United States
Recall initiated2025-06-30
Classified2025-07-30
Reported by FDA2025-08-06
DistributedNationwide (US)
Countries outside the USAR, AT, AU, BD, BE, BG, BH, BO, BR, BZ, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DZ, EC, EE, EG, ES, FI, FR, GB, GH, GR, HK, HN, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KE, KR, KW, KY, LB, LK, LT, LU, LV, MA, MT, MX, MY, NI, NL, NO, NP, NZ, OM, PA, PE, PH, PK, PL, PT, PY, QA, RO, RS, SA, SE, SG, SI, SK, SV, TH, TN, TT, TW, UA, VE, VN, ZA
Quantity294 units
UPC / GTIN / UDI-DI00884838095083, 00884838098909, 00884838105805
Serial numbers17006, 17172, 17204, 17206, 17212, 17215, 17222, 17237, 17238, 17239, 17240, 17242, 17245, 17246, 17247, 17250, 17252, 17258, 17260, 17264, 17265, 17266, 17268, 17269, 17271 and 269 more
Model numbers00884838095083, 00884838098909, 00884838105805, 781270, 782113, 782129

Product

SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;

Reason for recall

The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2216-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.