Z-2866-2018Class II

DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062

Name: Z-2866-2018 DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
Creator: Philips Medical Systems Gmbh, DMC
Published: 2018-06-27
License: https://open.fda.gov/license/

Philips Medical Systems DMC GmbH / initiated 2018-06-27 / Terminated / root cause: design

FDA source

Philips Medical Systems Gmbh, DMC began a recall of DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062 on 2018-06-27. FDA classified it as Class II and gives the reason as "The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2866-2018
Classification: Class II
Status: Terminated
Initiated: 2018-06-27
Posted: 2018-08-17
Terminated: 2024-04-30
Recalling firm: Philips Medical Systems DMC GmbH
Product: DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
Product code: MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Reason for recall: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
Root cause tag: design
FDA root cause: Device Design
Action: On June 27, 2018, Philips Medical Systems issued URGENT FIELD SAFETY NOTICES, Medical Device Recall letters to customers. Customers were encouraged to always check the right position of the hook and ensure that the hook is locked according tot he IFU. Press hook down until it is locked. Make sure that the hook is in position. A Philips Service Engineer will contact impacted customers as soon as the Field Action Kit is ready to be implemented. Should you need to communicate with Philips in regards to this program, please reference FCO-71200185. If you need further information or support concerning this issue, please contact your local Philips representative.
Distribution: US Nationwide; International to 66 countries
Product codes and lots: Serial Numbers: 386786/SN0702512 375366 416255/SN0902004 358322 388667/SN0802105 375367 397229/SN0802250 396838/SN0802365 386108/SN0802044 405687/SN0802469 354125 362438 406156/SN0802537 413697/SN0802634 402853/SN0902012 405889/SN0802629 383385/SN0802011 378827/SN0802021 384013/SN0702495 358017 358496 377925/SN0802060 356953 355621 357888 356956 368431 356963 406016/SN0802476 346522 375370 70700 351321 392504/SN0802182

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2866-2018
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2841-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2842-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2843-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2844-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2845-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2846-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2847-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2848-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2849-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2850-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2851-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2852-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2853-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2854-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2855-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2856-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2857-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2858-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2859-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2860-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2861-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2862-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2863-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2864-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2865-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2866-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2867-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17
Z-2868-2018	Class II	Terminated	Voluntary: Firm initiated	2018-08-29	2018-08-17

Product code MQB

K090625Class IIWireless Portable Detector Fd-W17Philips Medical Systems North America Co. / cleared 2009-03-24

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)