Linkbio Corp. 2023-06-07 Health serious FDA
Health · FDA · Recall #FDA-Z-1674-2023
LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 … Recall
Issued June 7, 2023 · Linkbio Corp.
In June 2023, Linkbio Corp. recalled the LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 …, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).
What you should do
- 1 Stop using LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Linkbio Corp. 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
- Linkbio Corp.
- Category
- Health
- Recall date
- June 7, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TX
- Recall number
- FDA-Z-1674-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Linkbio Corp. has 7 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.