cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate.
FDA Recall Z-1610-2018 · Posted 2018-05-03
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Recalling FirmRoche Diagnostics Corporation
Recall StatusTerminated
Product CodeCEM
Date Initiated2018-02-22
Date Terminated2019-11-15
Product Quantity1026 total products
Reason for Recall
The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.
Firm Action
ROCHE sent an Urgent Medical Device Correction Letter dated February 22, 2018, via UPS to affected customers.
Customers were instructed to complete the following: " 1) Use the Return to Setup and Exit buttons to ensure execution of scheduled AutoQC measurements as described in this Urgent Medical Device Correction (UMDC); 2) Check to see if the next scheduled AutoQC measurement is performed to ensure the AutoQC scheduler is working as expected; 3) If your facility has distributed the affected product to another site, please ensure this UMDC is provided to that site; 4) Complete the attached fax form (TP-00146) and fax it to 1-844-491-7776 or scan and email to [email protected]; 5) File this UMDC for future reference.
Customers with questions should contact the Roche Support Network Customer Support Center, 24 hours a day, seven days a week at 1-800-526-2272.
Root Cause
Software design
Distribution Pattern
USA ( nationwide)
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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