Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label (component part number 11032). A software application used to help estimation of blood loss. Used with blood bearing canisters and accessories.
FDA Recall Z-1402-2022 · Posted None
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Recalling FirmStryker Instruments Div. of Stryker Corporation
Recall StatusTerminated
Product CodePBZ
Date Initiated2020-01-22
Date Terminated2024-01-29
Product Quantity16,700 units
Reason for Recall
Some Canister Scanning Labels used to calibrate the Triton Canister System have a color variance. Based on a comprehensive analysis, blood loss estimates obtained using these Canister Scanning Labels may result in lower than expected results.
Firm Action
Customers were notified via email dated 1/22/20.
We request the following actions from you:
1. Please confirm receipt of this communication by emailing myself and/or your Gauss representative.
2. Please identify any of these miscolored Canister Scanning Labels in your possession:
" Find the the miscolored labels by locating any package of insert + scanning label with a date of manufacture prior to to 2019-12-24. See an example below:
3. Once identified, please:
" Quarantine this product and indicate this has been completed by written email response to this communication
Your Gauss representative will be in contact with you this week to help resolve this issue. Replacement product will be provided immediately. Thank you for your attention to this matter. Please feel free to reach out directly to me if you have any questions.
Root Cause
Process control
Distribution Pattern
US Nationwide
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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