Home / Recalls / Philips Medical Systems Gmbh, DMC / Z-2851-2018

Z-2851-2018 Class II Terminated

Recalled by Philips Medical Systems Gmbh, DMC — Hamburg

FDA device recall Z-2851-2018 was initiated by Philips Medical Systems Gmbh, DMC on Jun 27, 2018 and is designated Class II. 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. The recall status is terminated (terminated Apr 30, 2024).

Recall Details

Product Type
Devices
Report Date
Aug 29, 2018
Initiation Date
Jun 27, 2018
Termination Date
Apr 30, 2024
Voluntary/Mandated
Voluntary: Firm initiated

Product Description

DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027

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.

Distribution Pattern

US Nationwide; International to 66 countries

Code Information

Serial Numbers: SN17000294 SN17000295 SN17000114 SN17000185 SN17000362 SN17000263 SN17000264 SN17000399 SN15000017 SN17000235 SN18000001 SN17000414 SN17000376 SN16000352 SN17000311 SN17000070 SN14000079 SN14000080 SN17000044 SN17000346 SN14000052 SN17000045 SN17000351 SN17000038 SN17000262 SN17000126 SN15000122 SN17000100 SN17000422 SN17000359 SN16000390 SN15000048 SN17000084 SN16000386 SN17000106 SN17000288 SN17000278 SN17000335 SN16000394 SN16000387 SN17000151 SN17000352 SN17000329 SN17000349 SN17000303 SN17000334 SN17000216 SN17000305 SN17000398 SN15000328 SN17000289 SN17000411 SN17000436 SN17000090 SN15000006 SN17000179 SN17000034 SN17000231 SN16000355 SN17000166 SN17000127 SN16000421 SN16000398 SN14000105 SN16000430 SN16000418 SN17000150 SN17000092 SN15000054 SN15000097 SN15000110 SN17000373 SN15000132 SN14000040 SN14000045 SN15000098 SN16000435 SN15000142 SN15000151 SN17000141 SN15000410 SN15000417 SN16000402

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-2851-2018
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Other recalls by Philips Medical Systems Gmbh, DMC

  • Z-2357-2021 Class II — CombiDiagnost R90 Software Version R1.0 and R1.1 (Jul 22, 2020)
  • Z-1329-2020 Class II — CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray… (Dec 19, 2019)
  • Z-1328-2020 Class II — CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray… (Dec 19, 2019)
  • Z-0612-2019 Class II — Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030… (Nov 7, 2018)
  • Z-0239-2019 Class II — Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System… (Sep 19, 2018)
  • Z-2866-2018 Class II — DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062 (Jun 27, 2018)
  • Z-2862-2018 Class II — DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 (Jun 27, 2018)
  • Z-2841-2018 Class II — DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 (Jun 27, 2018)
  • Z-2861-2018 Class II — DigitalDiagnost Release 3 (Stitching Patient Support) 712025 (Jun 27, 2018)
  • Z-2858-2018 Class II — DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 (Jun 27, 2018)

FDA data resources