Official recall record
BD Facsduet™ Sample Preparation Systems
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-08-27
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Through a customer complaint investigation, BD identified a specimen volume bias issue with the BD Facsduet™ sample preparation system when using software version 1.4.1. When the multidispense feature is enabled in the BD Facsduet™ sample preparation system software, and the user is preparing a two-tube assay, the specimen volume dispensed into the first tube will be at least 3% higher than the specimen volume dispensed into the second tube. For assays, where absolute counts are calculated using BD Trucount™ tubes, an increase in the volume may result in higher-than-expected absolute counts in the first tube compared to the second tube. This issue will be observed when preparing the following assays on the BD Facsduet™ sample preparation system: 1. BD Multitest™ IMK kit with BD Trucount™ tubes. note: if using the BD Multitest™ IMK kit with BD Trucount™ tubes, a QC message will appear on your report if the bias is outside the acceptable range per assay requirements. 2. BD Multitest™ 6-color TBNK with BD Trucount™ tubes only if consecutive replicates of two are run. 3. for all other quantitative assays utilizing BD Trucount™ tubes in consecutive replicates of two, please follow your institution's procedures to determine if a review of reported results is necessary. This issue does not affect assays that are determining percent positive, semi quantitative information. Recall start date: August 12, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.