FDAClass IIFebruary 18, 2015

Athrosurface 40mm 13.75x31mm Taper Post Fixation recall

Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic…

Why was Athrosurface 40mm 13.75x31mm Taper Post Fixation recalled?

Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.

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: 8135-1875 Part Number: 3135-1875

Product
Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic…
Recalling firm
Arthrosurface, Inc.
Quantity
182 units
Distribution
Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
Recall date
February 18, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls