Class 2 Device Recall Dimension Gentamicin Flex reagent cartridge

• Date Initiated by Firm: April 19, 2018
• Create Date: June 13, 2018
• Recall Status: Terminated on April 24, 2020
• Recall Number: Z-2181-2018
• Recall Event ID: 80009
• 510(K)Number: K962819 K062024
• Product Classification: Enzyme immunoassay, gentamicin - Product Code LCD
• Product: Dimension Gentamicin Flex reagent cartridge, DM GENT, gentamicin enzyme immunoassay, Lot numbers affected are EB8115, BB8159, and FB8275.
• Code Information: Lots EB8115 BB8159 FB8275
• Recalling Firm/ Manufacturer: Siemens Healthcare Diagnostics, Inc.; 500 Gbc Dr Ms 514; Po Box 6101; Newark DE 19702-2466
• For Additional Information Contact: 800-441-9250
• Manufacturer Reason for Recall: The affected lots may exhibit inaccuracy for Quality Control and patient samples at the low end of the Analytical Measurement Range. The bias is due to the calibration curve not showing separation between the Level 1 and Level 2 calibrators.
• FDA Determined Cause: Under Investigation by firm
• Action: On April 19, 2018, the firm sent an Urgent Medical Device Recall letter to customers. The letter identified the affected lots and advised customers to do the following: Inspect stock, discontinue use of and discard the Dimension and Dimension Vista GENT lots listed in Table 1. ¿ Please review this letter with your Medical Director. ¿ Review your inventory of these products to determine your laboratorys replacement needs and to provide information to Siemens for reporting to the regulatory authorities. ¿ Complete and return the Field Correction Effectiveness Check Form attached to this letter within 30 days. ¿ If you have received any complaints of illness or adverse events associated with the product listed in Table 1, immediately contact your local Siemens Customer Care Center or your local Siemens Technical Support Representative.
• Quantity in Commerce: 7543
• Distribution: Nationwide distribution. Foreign distribution to Argentina, Australia, Brazil, Bahamas, Canada, Germany, India, Japan, Myanmar, New Zealand, Saudi Arabia, Taiwan, and South Africa.
• 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 = LCD and Original Applicant = DADE BEHRING, INC.; 510(K)s with Product Code = LCD and Original Applicant = DADE INTL., INC.