Exactech, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1031-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.

Product Classification:

Class II

Date Initiated: November 7, 2016

Date Posted: January 25, 2017

Recall Number: Z-1031-2017

Event ID: 75989

Reason for Recall:

Products were labeled with incorrect Global Trade Item Numbers. The GTIN on the label identifies the devices as another.

Status: Terminated

Product Quantity: 12 devices

Code Information:

Serial No. 4507932-4507943; Catalog No. 138-36-29; UDI: 10885862024831

Distribution Pattern:

AZ, CA, CO, FL, IL, KS, MD, NJ, NY, OH, OK, TN, & VA; Germany, Italy, Japan, Spain, & Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated