Philips MX 16-Slice CT Scanner System — Class II medical device recall Z-0899-2013
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2013-03-06, distributed in AL, AR, CA, FL, GA, IL, IN, KY…. The four screws that secure the patient table top to the carrier became loose, which caused the table top to d
| Recall number | Z-0899-2013 |
|---|---|
| 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 | 2012-12-19 |
| Classified | 2013-02-28 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2013-12-03 |
| Distributed | AL, AR, CA, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NV, NY, OH, PA, PR, VA |
| Quantity | 412 units |
| Reason classes | device malfunction |
| Serial numbers | EP16E090001, EP16E090002, EP16E090003, EP16E090004, EP16E090006, EP16E090007, EP16E090008, EP16E090009, EP16E090010, EP16E090011, EP16E090012, EP16E090013, EP16E090015, EP16E100001, EP16E100004, EP16E100005, EP16E100006, EP16E100007, EP16E100008, EP16E100010, EP16E100011, EP16E100012, EP16E100013, EP16E100015, EP16E100016 and 387 more |
Product
Philips MX 16-Slice CT Scanner System, a whole-body computed tomography X-ray system.
Reason for recall
The four screws that secure the patient table top to the carrier became loose, which caused the table top to detach.
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-0899-2013. 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.