Patient Support Material Number: 9890 010 87431 used with:… — Class II medical device recall Z-0364-2016
Terminated recall by Philips Medical Systems, Inc., reported 2015-12-09, distributed in AZ, CT, FL, HI, KY, MA, MN, NC…. The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing
| Recall number | Z-0364-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems, Inc., Andover, MA, United States |
| Recall initiated | 2014-08-19 |
| Classified | 2015-12-03 |
| Reported by FDA | 2015-12-09 |
| Terminated | 2016-06-14 |
| Distributed | AZ, CT, FL, HI, KY, MA, MN, NC, TX, VA, WY |
| Countries outside the US | AR, AT, AU, CA, CH, DE, DK, ES, NL, RU, SA, SG |
| Quantity | 1,517 systems |
| Model numbers | 704060/706037 |
Product
Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost ; Model: 704060/706037
Reason for recall
The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.
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-0364-2016. 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.