Recall StatusTerminated
Date Initiated2018-07-11
Date Terminated2020-08-11
Product Quantity168919
Reason for Recall
The slides failed to meet current claims for Limit of Blank (LoB), Limit of Detection (LoD) and Limit of Quantification (LoQ) for urine samples. The measuring range (15-300 mmol/L) for urine samples when tested with the Cl- slide is not affected. The current Cl- LoQ is 5 mmol/L and the LoQ determined by this investigation is 15 mmol/L.
Firm Action
On 7/11/18, Important Product Correction Notification letters were distributed to customers. The letters instructed customers to perform the following actions:
VITROS Cl- Slides and VITROS CREA Slides Instructions for Use will be updated to contain the revised information described in this letter; we will notify you upon availability. In the interim, retain a copy of this customer letter for your records.
Calibration Diskette and ADD Data Release Version (DRV) 5992 (and above) will support the revised measuring range for VITROS CREA Slides. We anticipate that DRV 5992 will be available beginning on July 28, 2018 by eConnectivity or will be sent via your normal Cal Disk or ADD mailing.
Prior to the availability of the revised IFU, be aware that if a serum or plasma sample contains a Triglyceride concentration of 600 mg/dL or higher, the Chloride result may be positively biased by approximately 2.1 mmol/L. Follow your normal laboratory procedures as you would for other known assay interferences. Note: It is acceptable to continue using VITROS Cl- Slides.
Upon availability, install the Calibration Diskette or ADD to implement the revised Measuring Range:
For VITROS 4600, 5600 or 5,1 FS Systems: Install ADD DRV 5992 or above, Select All Assay Data option
For VITROS 250/350 Systems: Install Calibration Diskette DRV 5992 or above
Refer to the enclosure for additional instructions to update the Measuring Range.
Update laboratory procedures and your Laboratory Information System (LIS), as necessary.
Retain this letter until we send a notification to alert you when the revised IFUs are available.
Complete the Confirmation of Receipt form and return by July 25, 2018.
Post this notification by each system that processes VITROS Cl- or CREA Slides.
Forward this notification if the product was distributed outside of your facility.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide Distribution - US Nationwide- The products were distributed to the following foreign countries: Australia, Belgium, Bermuda, Brazil, Canada, Chile, China, Columbia, Denmark, France, Germany, India, Italy, Japan, Mexico, Norway, Poland, Portugal, Russia, Singapore, Spain, Sweden, The Netherlands, and United Kingdom.
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.