FDAClass IIFebruary 25, 2015

Ringloc+ Acetabular Shell Finned 52 mm recall

Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.

Why was Ringloc+ Acetabular Shell Finned 52 mm recalled?

Biomet recalled the Mallory Head 4 Finned Acetabular Shell 50mm (Lot 364600) and Ringloc + Acetabular Shell Limited Hole Finned 52 mm (Lot 427840) following a mix up in packaging with the two.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Catalog Number: 16-104152 Lot Number Identification: 427840

Product
Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.
Recalling firm
Biomet, Inc.
Quantity
17
Distribution
Distributed in the states of VA and TX and the country of Japan.
Recall date
February 25, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls