Encore Medical, LP 2023-12-20 Health serious FDA
Health · FDA · Recall #FDA-Z-0532-2024
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device. Recall
Issued December 20, 2023 · Encore Medical, LP
In December 2023, Encore Medical, LP recalled the RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device., a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
What you should do
- 1 Stop using RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device. 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
- December 20, 2023
- Units affected
- Not reported
- Sold at
- U.S.: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, Puerto Rico, RI, SC, TN, TX, VA, and WA O.U.S.: None
- Recall number
- FDA-Z-0532-2024
- 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 903rd Health recall we've logged in 2023.