FDA Device recall Z-0364-2016
Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost
- FDA Device
- Class II
- terminated
- Published 2015-12-09
On 2015-12-09 the FDA classified a Class II recall of Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost by Philips Medical Systems, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0364-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-19 |
| Published | 2015-12-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Medical Systems |
| Distribution | AZ, CT, FL, HI, KY, MA, MN, NC, TX, VA, WY |
Product
Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost ; Model: 704060/706037
Reason
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.
Identifiers
| code_info | All patient support for stitching are affected. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0364-2016%22
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