Stryker, Inc. 2024-02-21 Health serious FDA
Health · FDA · Recall #FDA-Z-1085-2024
Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm Recall
Issued February 21, 2024 · Stryker, Inc.
In February 2024, Stryker, Inc. recalled the Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
What you should do
- 1 Stop using Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Stryker, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Stryker, Inc.
- Category
- Health
- Recall date
- February 21, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
- Recall number
- FDA-Z-1085-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Stryker, Inc. has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.