Encore Medical, LP 2025-07-02 Health serious FDA
Health · FDA · Recall #FDA-Z-2008-2025
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm … Recall
Issued July 2, 2025 · Encore Medical, LP
In July 2025, Encore Medical, LP recalled the Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm …, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
What you should do
- 1 Stop using Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Encore Medical, LP 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
- Encore Medical, LP
- Category
- Health
- Recall date
- July 2, 2025
- Units affected
- Not reported
- Sold at
- At time of quarantine: RFK Medical Inc. Virginia (VA) CE102 506-04-122 5035A1018 ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm 2
- Recall number
- FDA-Z-2008-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Encore Medical, LP has 6 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.