Z-2561-2025 Class II Ongoing
FDA device recall Z-2561-2025 was initiated by Exactech, Inc. on August 15, 2025 and is designated Class II. Reason for recall: Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling. The recall status is ongoing. Affected quantity: 61,334 UNITS.
Recall Details
- Product Type
- Devices
- Report Date
- September 24, 2025
- Initiation Date
- August 15, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 61,334 UNITS
Product Description
Exactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE 38MM HUM LINER +2.5/ 320-42-00,145-DEG PE 42MM HUM LINER +0/ 320-42-03,145-DEG PE 42MM HUM LINER +2.5/
Reason for Recall
Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.
Distribution Pattern
Worldwide - US Nationwide distribution in the states of CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MN, NV, NY, OH, OK, PR, SC, TN, TX, VA, WI and the countries of Australia, Austria, Brazil, Canada, Colombia, France, United Kingdom, Guatemala, India, Italy, Japan, Korea, Germany, The Netherlands, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, Dubai.
Code Information
All Serial Numbers, REF: 320-38-00/UDI:10885862086655 REF: 320-38-03/UDI: 10885862086662 REF: 320-42-00/UDI: 10885862086693 REF: 320-42-03/UDI: 10885862086709