Arthrex, Inc. 2022-05-11 Health serious FDA
Health · FDA · Recall #FDA-Z-1035-2022
K-Wire, 1.35 mm x 170 mm Recall
Issued May 11, 2022 · Arthrex, Inc.
In May 2022, Arthrex, Inc. recalled the K-Wire, 1.35 mm x 170 mm, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Products do not meet length and diameter specifications.
What you should do
- 1 Stop using K-Wire, 1.35 mm x 170 mm right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Arthrex, 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
- Arthrex, Inc.
- Category
- Health
- Recall date
- May 11, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide distribution in the states of OH, TN, MO, LA, IA, AZ, PA, NY, OR and the countries of to Belgium, Egy
- Recall number
- FDA-Z-1035-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Arthrex, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.