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Open, Classified

ddR Formula B X-ray System, ddR Formula B Product Usage: X-ray system used for imaging

FDA Recall Z-3248-2018 · Posted 2018-09-25

Recalling FirmSwissray Medical
Recall StatusOpen, Classified
Product CodeKPR
Date Initiated2016-08-09
Product Quantity26 units

Reason for Recall

Possible injury due to movement of the arm, calibration loss and communication loss.

Firm Action

November 2016, Swissray Medical issued official communication to customers as a Action Notification Report. The manufacturer, Swissray Medical AG, distributed the Work Instructions for the FCO and the Action Notification Report Form to all distributors and service entities who would be performing corrective actions in the field. The Swissray Field Engineer then presented the Report to the customer (end user facility) and communicated with the customer in-person while performing the corrective action on-site. When corrective actions were completed, both the customer and service personnel then sign the Report to confirm that the customer was informed about the corrective action and that corrective action was completed.

Root Cause

Device Design

Distribution Pattern

US Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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