Data Foundry

Medical device recalls 2016

Ingenuity Core Model No — Class II medical device recall Z-2383-2016

Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2016-08-17, distributed in AK, AL, AR, AZ, CA, CO, CT, DE…. Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips Brilliance 64 and Ingenuity CT products

Recall numberZ-2383-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmPhilips Medical Systems (Cleveland) Inc, Cleveland, OH, United States
Recall initiated2016-04-29
Classified2016-08-10
Reported by FDA2016-08-17
Terminated2018-07-02
DistributedAK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WV, WY
Countries outside the USAE, AR, AT, AU, BD, BE, BO, BR, CH, CN, CO, DE, EE, ES, FI, FR, GB, ID, IE, IL, IN, IT, JO, JP, KR, LB, LT, LV, MY, NL, NO, NZ, PA, PH, PL, PT, SE, SK, TH, TR, TW, VN, ZA
Quantity276 units
Reason classessoftware
Model numbers132164, 132465, 310001, 310002, 310003, 310009, 310017, 310019, 310022, 310023, 310026, 310032, 310039, 310042, 310052, 310054, 310055, 310059, 310064, 310069, 310070, 310071, 310081, 310087, 310088 and 289 more

Product

Ingenuity Core Model No. 728321; To produce cross-sectional images of the body.

Reason for recall

Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips Brilliance 64 and Ingenuity CT products that could affect the performance of the equipment.

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-2383-2016. 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.