Stryker recalls specific Trevo Trak 21 Microcatheter models due to missing product drawing on carton labels. This may affect medical device safety during procedures.
Microcatheter product label on the carton is missing the microcatheter product drawing/illustration.
Stryker is recalling certain Trevo Trak 21 Microcatheter models because the carton labels lack the required product drawing. This could lead to confusion during medical procedures if healthcare providers cannot identify the correct device.
The missing product drawing on the carton label could cause healthcare providers to use the wrong microcatheter during procedures. This might lead to incorrect device placement or complications if the wrong device is selected.
Healthcare professionals using these microcatheters for medical procedures are most at risk. Patients receiving these devices during diagnostic or therapeutic procedures may be affected if the wrong device is used.
Check for the product codes: REF 90338, 91412, 91413, 91414, 91415, SFP914170, or SFP914190. These models were sold with specific lot numbers and reference codes.
Look for the product drawing on the carton label to confirm the microcatheter model.
The recall is due to missing product drawing on the carton label, which could lead to confusion during medical procedures.
Trevo Trak 21 Microcatheter (REF 90338), TREVO NXT 3X32+TRAK21 2-PACK (REF 91412), TREVO NXT 4X28+TRAK21 2-PACK (REF 91413), and other specific models with the listed reference codes.
No action is required beyond checking the product label for the missing drawing. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1386-2022 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1386-2022 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
