Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported August 29, 2018
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
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.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Philips Medical Systems Gmbh, Dmc recalled DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 - a moderate-severity action.
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 was recalled by Philips Medical Systems Gmbh, Dmc in August 29, 2018. Reason: The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or…. Check the official notice for the remedy. Verify recall #Z-2859-2018 with the FDA Devices before acting.
The recall
Philips Medical Systems Gmbh, Dmc issued this moderate-severity FDA Devices recall-The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or….
- Moderate
- severity level
- Class II
- classification
- August 29, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2859-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2859-2018) was formally reported on August 29, 2018, with the manufacturer initiating the action on June 27, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Philips Medical Systems Gmbh, Dmc is listed as the recalling firm, operating out of Hamburg. The number of affected units is not disclosed in the agency filing, which is common for drug and food recalls where lot-level tracking supersedes unit counts.
The documented reason for this recall is: 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 data in the federal record shows the product reached: US Nationwide; International to 66 countries. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
Unknown
Related Recalls
6
0 from same agency
Product description
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2859-2018 |
| Date reported | August 29, 2018 |
| Date initiated | June 27, 2018 |
| Recalling firm | Philips Medical Systems Gmbh, Dmc |
| Firm location | Hamburg |
| Affected scope | Not disclosed |
| Distribution | US Nationwide; International to 66 countries |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2859-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022. Recalled by Philips Medical Systems Gmbh, Dmc.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 29, 2018. Severity: Moderate. Recall number: Z-2859-2018.
Where was the recalled product distributed? ▼
Distribution: US Nationwide; International to 66 countries.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2859-2018) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported August 29, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.