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U.S. Department of Health and Human Services

Class 2 Device Recall Atellica IM 1300 Analyzer

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  Class 2 Device Recall Atellica IM 1300 Analyzer see related information
Date Initiated by Firm September 28, 2021
Create Date October 16, 2021
Recall Status1 Open3, Classified
Recall Number Z-0124-2022
Recall Event ID 88792
510(K)Number K151792  
Product Classification Analyzer, chemistry (photometric, discrete), for clinical use - Product Code JJE
Product Atellica IM 1300 Analyzer, SMN 11066001
Code Information All units
Recalling Firm/
Manufacturer		 Siemens Healthcare Diagnostics, Inc
333 Coney St
East Walpole MA 02032-1516
For Additional Information Contact
508-668-5000
Manufacturer Reason
for Recall		 Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600 analyzers may overflow when pierced while on an analyzer located at an altitude of greater than 350m (1148ft) above sea level. As a result, customers at these altitudes may observe an increased number of Reagent Volume Check Errors.
FDA Determined
Cause 2		 Under Investigation by firm
Action On September 27, 2021, the firm initiated notifications to affected customers. Customer distribution included all customers located in a city at an altitude of 350 meters (1148 feet) or higher. Customers were informed that Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600 analyzers may overflow when pierced while on an analyzer located at an altitude of greater than 350 (m) or 1148 (ft) above sea level. The letters provide directions for mitigating the potential for leakage. If you have any questions, contact your local Siemens Healthineers technical support representative.
Quantity in Commerce 1193
Distribution Domestic distribution to AZ CA CO GA ID KS MO MT NC NE NM NV OH OK OR PA TN TX UT VA WA WI WY. Foreign distribution worldwide.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = JJE and Original Applicant = Siemens Healthcare Diagnostics,Inc.
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