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Zimmer Biomet, Inc. recalls PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System
Recalled January 10, 2018 · FDA recall Z-0312-2018 · Zimmer Biomet
Hazard
Device was distributed with the etching missing from the product. · FDA Class II
Units
15 units
Sold at
Distributed domestically to MI, MN, ND.
Description
Device was distributed with the etching missing from the product.
Product
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.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →