Medacta Usa Inc 2023-04-26 Health serious FDA
Health · FDA · Recall #FDA-Z-1400-2023
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device Recall
Issued April 26, 2023 · Medacta Usa Inc
In April 2023, Medacta Usa Inc recalled the MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
There is a potential for breakage of the small screw used to affix the anti-backout plate.
What you should do
- 1 Stop using MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medacta Usa 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
- Medacta Usa Inc
- Category
- Health
- Recall date
- April 26, 2023
- Units affected
- Not reported
- Sold at
- US: ID, TX, GA, VA, AZ
- Recall number
- FDA-Z-1400-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Medacta Usa Inc 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.