FDA Medical Device Recalls (openFDA)
Ortho-Clinical Diagnostics, Inc.: The VITROS XT Chemistry Products ALB-TP Slides is a single device that contains both an albumin test and a total protein test side by side separated by a plastic barrier sealed within a single slide frame. In this format, individual reactions occur, and test results are generated for each analyte independently of the other analyte. The ALB test is a multilayered, analytical element coated on a polyester support. For the albumin measurement, a drop of patient sample is deposited on the slide and is evenly distributed by the spreading layer to the underlying layers. When the fluid penetrates the reagent layer, the bromocresol green (BCG) dye diffuses to the spreading layer and binds to albumin in the sample. This binding results in a shift in wavelength of the reflectance maximum of the free dye. The color complex that forms is measured by reflectance spectrophotometry. The amount of albumin-bound dye is proportional to the concentration of albumin in the sample. Model/Catalog Number: 6844293
- Recall number
- Z-2684-2024
- Recalling firm
- Ortho-Clinical Diagnostics, Inc.
- Product
- The VITROS XT Chemistry Products ALB-TP Slides is a single device that contains both an albumin test and a total protein test side by side separated by a plastic barrier sealed within a single slide frame. In this format, individual reactions occur, and test results are generated for each analyte independently of the other analyte. The ALB test is a multilayered, analytical element coated on a polyester support. For the albumin measurement, a drop of patient sample is deposited on the slide and is evenly distributed by the spreading layer to the underlying layers. When the fluid penetrates the reagent layer, the bromocresol green (BCG) dye diffuses to the spreading layer and binds to albumin in the sample. This binding results in a shift in wavelength of the reflectance maximum of the free dye. The color complex that forms is measured by reflectance spectrophotometry. The amount of albumin-bound dye is proportional to the concentration of albumin in the sample. Model/Catalog Number: 6844293
- Status
- Open, Classified
- Initiated
- 2024-07-10
- Posted
- 2024-08-16
- Terminated
- not on file
- Reason
- The reason for this recall is QuidelOrtho has determined that during normal use the VITROS XT ALB-TP Slides may shed dust and debris as they travel through the MicroSlide Subsystem of the VITROS XT 3400 or VITROS XT 7600 analyzer. This dust and debris may then settle onto VITROS Na+ (Sodium) Slides as they are processed through the same MicroSlide Subsystem, potentially resulting in an increase in non-reproducible, positively, or negatively biased Na+ results. The level of bias will depend on where the dust and debris settle on the Na+ MicroSlide and may impact Na+ measurements to varying degrees inside and outside of the measuring range depending on the amount of contamination. All of which could vary from no/low bias with no patient harm, to extreme bias (falsely elevated or reduced results) potentially resulting in incorrect diagnosis; treatment; and/or a serious patient health hazard (for example, hypernatremia or hyponatremia). This issue may also potentially generate error codes preventing the analyzer from processing the MicroSlide Assays and cause delay of the patient results. All current and expired VITROS XT Chemistry Products ALB-TP slides are affected by this issue.
- Root cause
- Under Investigation by firm
- Action
- QuidelOrtho issued Urgent Product Correction Notification Letter to Distributors and End-Users on 10 July 2024, (Ref. CL2024-139) via FedEx overnight courier and/ or electronically using ORTHO PLUS e-Communications to customers who have been shipped VITROS XT Chemistry Products ALB-TP slides in the last 24 months. Letter states reason for recall, health risk and action to take: Until this issue is resolved, QuidelOrtho will be pausing availability of the VITROS XT ALB-TP Slides and we will shift all affected customers to the individual VITROS Chemistry Products ALB Slides and VITROS Chemistry Products TP Slides. We have verified through internal testing that the individual ALB and TP slides do not show the same behavior as the XT ALB-TP slides. Upon receipt of this notification, please perform the cleaning steps listed in Appendix 1: VITROS XT System Cleaning Focus, on your VITROS XT 3400 and/or XT 7600 System(s) to remove any dust and debris which may have accumulated in the MicroSlide Subsystem. Perform the cleaning steps listed in Appendix 1: VITROS XT System Cleaning Focus again on your VITROS XT 3400 and/or XT 7600 System(s) after your laboratory has discontinued using VITROS XT ALB-TP Slides. Customers may continue to use VITROS XT ALB-TP Slides until the replacement VITROS ALB Slides and VITROS TP Slides are received. After receipt of the replacement VITROS Slides, and on completion of any necessary crossover studies / validation, please discontinue using, render unusable, and discard your remaining inventory of VITROS XT ALB-TP Slides. cleaning of the MicroSlide Subsystem on your VITROS XT 3400 and/or VITROS XT 7600 System(s). Refer to Appendix 1: VITROS XT System Cleaning Focus for a list of specific areas which have been observed to accumulate dust and debris shed from VITROS XT ALB-TP Slides. " Prepare your laboratory s transition from using VITROS XT ALB-TP Slides to the VITROS Chemistry Products ALB Slides and VITROS TP Slides products, including
- Quantity
- 88253 units
- Distribution
- Nationwide. Foreign: Australia Belgium Bermuda Brazil Canada L3R 0B8 Chile China Colombia Denmark France Germany India Italy Japan Mexico Norway Portugal Russia Singapore 609917 Spain Sweden The Netherlands United Kingdom
- Lot, serial or model codes
- UDI/GTIN# 10758750031771 All current and expired coatings
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- CIX
- Firm FEI
- 1000136573
- Firm city
- Rochester
- Firm state
- NY
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28