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

T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. 2023-07-12 Health serious FDA
Health · FDA · Recall #FDA-Z-2065-2023

Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation… Recall

Issued July 12, 2023 · T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

In July 2023, T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. recalled the Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes potential of injury.

What you should do

  1. 1 Stop using Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. 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
T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
Category
Health
Recall date
July 12, 2023
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Japan, Netherlands.
Recall number
FDA-Z-2065-2023
Made in
Israel
Issuing agency
FDA

In context

  • T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. has 1 recall 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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