Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PPS RingLoc+ Acetabular Shell Recalled by Zimmer Biomet, Inc. Due to Device was distributed with the etching missing from...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended to replace the natural acetabulurn damaged by disease, trauma or revision of previous arthroplasty. The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended for uncemented use only.
Quantity: 15 units
Why Was This Recalled?
Device was distributed with the etching missing from the product.
Where Was This Sold?
This product was distributed to 3 states: MI, MN, ND
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report