FDAClass IISeptember 9, 2015

Vision RingLoc Shell 50 mm recall

Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.

Why was Vision RingLoc Shell 50 mm recalled?

The device was assembled without screw hole plugs.

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?

Part Number:135250; Lot Number:946410

Product
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
Recalling firm
Biomet, Inc.
Quantity
5
Distribution
Distributed in Canada and Japan.
Recall date
September 9, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
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