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Terminated

Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60 & ADAC CARDIO C60) Nuclear gamma cameras intended to produce images depicting the anatomical distribution of single photon and positron emitting radioisotopes with the human body for interpretation by medical personnel.

FDA Recall Z-1607-2015 · Posted 2015-05-13

Recall StatusTerminated
Product CodeLMC
Date Initiated2015-03-11
Date Terminated2018-06-26
Product Quantity975 units

Reason for Recall

The firm was notified by a customer that the collimator exchange carriage and the collimator storage cabinet were misaligned.

Firm Action

Philips sent an Urgent - Medical Device Correction letter dated March 12, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. The firm requested their customers to do the following: " If a misalignment on the top and/or bottom of the guide rail between the cabinet and carriage can be visually detected do not continue with the collimator exchange procedure, " If the misalignment is visually detected, be aware that the customer/user cannot remedy this issue and will require service interaction prior to the continued use of the system. " This letter should be placed in your User Documentation until otherwise notified. If you need any further information or support concerning this issue, please contact your local Philips Healthcare representative: For North America and Canada contact the Customer Care Solutions Center (1-800-722-9377, Option 5: Enter site ID or follow the prompts).

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution - US (nationwide) to the states of: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY., and to the countries of : Australia, Austria, Belgium, Brazil, Canada, China, Costa Rica, Egypt, France, Germany, Hong Kong, Ireland, Italy, Japan, Korea, Lebanon, Netherlands, Norway, Pakistan, Portugal, Russia, Singapore, South Korea, Spain,Thailand and United Kingdom.

Official Source

View FDA Recall →

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

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