FDAJune 29, 2017device

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...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Device was distributed with the etching missing from the product.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00880304593169

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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... — Recall Details · AllClear