MX 16-Slice CT Scanner System — Class II medical device recall Z-0019-2014
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2013-10-23, distributed in AL, AR, CA, FL, GA, IL, IN, KY…. A pinch point at the end of the table top can cause injury.
| Recall number | Z-0019-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems (Cleveland) Inc, Cleveland, OH, United States |
| Recall initiated | 2013-07-22 |
| Classified | 2013-10-17 |
| Reported by FDA | 2013-10-23 |
| Terminated | 2014-09-25 |
| Distributed | AL, AR, CA, FL, GA, IL, IN, KY, MS, NC, NJ, NV, NY, OH, PA, VA |
| Countries outside the US | AR, AT, AU, BE, BO, BR, CH, CN, DZ, ES, GH, GR, ID, IE, IN, IT, JO, KR, LB, LT, LV, MX, NL, NP, OM, PH, PL, PT, RO, RU, SA, SG, TH, TR, UA, VE, VN, ZA |
| Quantity | 326 |
| Serial numbers | EP16E090001, EP16E090002, EP16E090003, EP16E090006, EP16E090009, EP16E090010, EP16E090011, EP16E090012, EP16E090013, EP16E090015, EP16E100001, EP16E100004, EP16E100006, EP16E100008, EP16E100010, EP16E100012, EP16E100013, EP16E100016, EP16E100017, EP16E100018, EP16E100019, EP16E100020, EP16E100021, EP16E100022, EP16E100023 and 301 more |
| Model numbers | 510, 728131 |
Product
MX 16-Slice CT Scanner System. Used as a whole-body computed tomography X-Ray system.
Reason for recall
A pinch point at the end of the table top can cause injury.
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-0019-2014. 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.