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Serious recall: Injury is possible or has been reported. Take action promptly.

Wright Medical Technology, Inc. 2023-07-12 Health serious FDA
Health · FDA · Recall #FDA-Z-2105-2023

Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile. Recall

Issued July 12, 2023 · Wright Medical Technology, Inc.

In July 2023, Wright Medical Technology, Inc. recalled the Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile., a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes.

What you should do

  1. 1 Stop using Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile. right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Wright Medical Technology, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Wright Medical Technology, Inc.
Category
Health
Recall date
July 12, 2023
Units affected
Not reported
Sold at
There was no U.S. distribution, including government and military. Foreign distribution was made to Australia, Belgium, Canada, Chile, Ch
Recall number
FDA-Z-2105-2023
Made in
United States
Issuing agency
FDA

In context

  • Wright Medical Technology, Inc. has 3 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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