Recall Ledger

Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)

Medical deviceClass IIOngoing

Summary: Encore Medical, LP is recalling Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036. Reason: Knee and Humeral socket implants contain incorrect labeling.

What is being recalled

Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036

Why

Knee and Humeral socket implants contain incorrect labeling.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the states of VA, TN, IL, IN, MI, CO, WY, MT, RI, MA, NJ, PA, MO, OK, LA, FL, CA. (states named: California, Colorado, Florida, Illinois, Indiana, Louisiana, Massachusetts, Michigan, Missouri, Montana, New Jersey, Oklahoma, Pennsylvania, Rhode Island, Tennessee, Virginia, Wyoming)

How to tell if yours is affected

Lot Code: Lot: 378P1382 GTIN: 00888912144544

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1460-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJanuary 15, 2026
ReportedMarch 4, 2026
CompanyEncore Medical, LP
Company locationAustin, TX, United States
Initiated byVoluntary: Firm initiated
Quantity20 implants

More recalls from Encore Medical, LP · all medical device recalls · recalls from January 2026

Official FDA record