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U.S. Department of Health and Human Services

Class 2 Device Recall Kodak Direct View DR 7500 System

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  Class 2 Device Recall Kodak Direct View DR 7500 System see related information
Date Initiated by Firm March 06, 2007
Date Posted June 30, 2007
Recall Status1 Terminated 3 on June 29, 2007
Recall Number Z-0738-2007
Recall Event ID 38233
510(K)Number K051258  
Product Classification X-Ray System - Product Code KPR
Product Kodak Direct View DR7500 System, Catalog #s 855-1046, 879-1345, 161-9139 --- A stationary X-Ray System. Device Listing # E222512.
Code Information Serial Numbers DR75000103, DR75000110, DR75000123, DR75000125, DR75000126, DR75000129, DR75000133, DR75000134, DR75000135, DR75000138, DR75000139, DR75000141, DR75000144, DR75000145, DR75000147, DR75000202, DR75000203, DR75000205, DR75000206,  DR75000210, DR75000213, DR75000219, DR75000220, DR75000221, DR75000232, DR75000250, DR75000252, DR75000258.
Recalling Firm/
Manufacturer		 Carestream Health, Inc.
1049 West Ridge Road
Rochester NY 14615
For Additional Information Contact Ms. Christine E. Ehmann
585-724-4487
Manufacturer Reason
for Recall		 The x-ray systems do not indicate the field size when the system's detector is turned off and the collimator is in manual mode. This results in the systems being noncompliant with the field indication performance standards of section 1020.31(e)(2)& (3) of 21Code of Federal Regulations (CFR).
FDA Determined
Cause 2		 Other
Action On 2/21/07, Eastman Kodak notified CDRH of its proposed Corrective Action Plan CAP). The CAP was approved by CDRH under the following conditions: (1) Kodak will visit each user facility, and apply dial indicator labels to the collimator knobs, apply a field size label to the collimator housing, and verify that each system complies with the field indication performance standard. (2) Kodak will prepare adequate instructions for the assembly/installation and testing of the dial indicators labels and field size labels. These instructions are to be furnished to all owners of the Kodak Direct View DR 7500 Systems. (3) Kodak will supplement the Kodak DR 7500 system product report with a copy of the adequate instructions. (4) Kodak will perform 100% verification of the recall effectiveness. (5) Kodak will not charge for the corrections and will reimburse the owner for any out-of-pocket expenses. (6) Kodak will notify the manufacturer of the Ralco 302 ACS collimators, Ralco, that the collimator is noncompliant with the performance standard. Kodak has reported that the CAP was completed as of 5/07/07.
Quantity in Commerce Domestic: 28 units
Distribution Nationwide: CO, IL, MI, MN, MS, NY, OK, PA, SC, TN, WA
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = KPR and Original Applicant = EASTMAN KODAK COMPANY
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