Tina-quant D-Dimer Test System, Fibrinogen/Fibrin Degradation Products Assay, Material Numbers 03001245322 - (cobas c 311, 501 and 502; INTEGRA 400 plus), 08105618190 - (cobas c 303 and 503)
FDA Recall Z-0352-2024 · Posted 2023-11-20
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Recalling FirmRoche Diagnostics Operations, Inc.
Recall StatusOpen, Classified
Product CodeGHH
Date Initiated2023-10-03
Product Quantity5,263 kits
Reason for Recall
Elevated results were detected with Li-heparin plasma samples when compared to citrated plasma samples.
Firm Action
An URGENT MEDICAL DEVICE CORRECTION notification letter dated 10/3/23 was sent to customers.
Actions Required
" Roche recommends using citrated plasma for D-Dimer quantification until further notice.
" If your laboratory continues to use Li-heparin plasma for D-Dimer quantification, you are required to confirm all results between 0.5 g FEU/mL and 0.675 g FEU/mL with another D-Dimer method or with a citrated plasma sample.
" If your laboratory continues to use Li-heparin plasma for D-Dimer quantification and chooses to confirm results with another method, you may request credit for that testing from Roche. Contact your Roche sales representative to request reimbursement.
" Please complete all sections of the Recall Response Form (TP-01981) enclosed with this UMDC and fax it to 1-844-491-7776 or email it to [email protected].
" File this Urgent Medical Device Correction (UMDC) for future reference.
Credit for Confirmatory Testing
If your laboratory continues to use Li-heparin plasma for D-Dimer quantification and chooses to confirm results with another method, you may request credit for that testing from Roche. Contact your Roche sales representative to request reimbursement.
Distributor Actions Required
" Read the enclosed Customer UMDC TP-01986.
" Within 14 days from receipt of this UMDC, distribute a copy of the enclosed Customer UMDC
TP-01986 to all customers to whom you have shipped the Tina-quant D-Dimer assays listed above in the last 2 years.
" Please complete all sections of the Distributor Recall Response Form (TP-01985) enclosed with this UMDC and fax it to 1-844-491-7776 or email it to [email protected].
" File this UMDC and the enclosed Customer UMDC for future reference.
Questions
Please contact the Roche Support Network Customer Support Center, 24 hours a day, seven days a week at 1-800-428-2336 if you have questions about the information contained in this UMDC.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution.
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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