Arthrosurface, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1113-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.

Product Classification:

Class II

Date Initiated: November 24, 2014

Date Posted: February 18, 2015

Recall Number: Z-1113-2015

Event ID: 69723

Reason for Recall:

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

Status: Terminated

Product Quantity: 182 units

Code Information:

Catalog Number: 8135-1875 Part Number: 3135-1875

Distribution Pattern:

Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.

Voluntary or Mandated:

Voluntary: Firm initiated