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Terminated

AccuSeed DS Digital Stepper, an accessory to a prostate radiation treatment planning system. Model #DS300

FDA Recall Z-0221-2007 · Posted 2006-11-29

Recall StatusTerminated
Product CodeITX
Date Initiated2006-11-09
Date Terminated2007-11-30
Product Quantity62 steppers

Reason for Recall

The In/Out adjustment knob can be over-turned, ultimately causing the incorrect placement of radioactive seeds in the patient.

Firm Action

The recalling firm issued letters dated 11/9/06 via regular mail. The letter informs the customer of the problem and includes an advisory notice instructing them to perform a test prior to each use. If the system does not function correctly, it can still be used safely in a manual mode until it can be returned for repair. A questionnaire was enclosed that will facilitate the firm in prioritizing repairs and retrofits. After the questionnaire is reviewed, the firm will contact the customer for further information regarding their facilities use of the device. This letter was also issued to the CMS customer support departments in Japan, China, and Europe, who will notify the foreign customers and prioritize their returns for repair.

Root Cause

Other

Distribution Pattern

Worldwide, including USA, Australia, Japan, China, France, Germany and Brazil.

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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