Data Foundry

Medical device recalls 2025

Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX… — Class II medical device recall Z-2011-2025

Ongoing recall by Encore Medical, LP, reported 2025-07-02, distributed in CO, FL, IL, IN, KY, MA, MI, MN…. Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included pro

Recall numberZ-2011-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmEncore Medical, LP, Austin, TX, United States
Recall initiated2025-05-28
Classified2025-06-23
Reported by FDA2025-07-02
DistributedCO, FL, IL, IN, KY, MA, MI, MN, NC, ND, OH, RI, TN, TX, UT, VA, WI, WV
Quantity200 units
Reason classeslabeling
UPC / GTIN / UDI-DI00190446829867
Lot numbers5039A1015, 5039A1021
Model numbers506-04-130

Product

Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm Model/Catalog Number: 506-04-130 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for use. While total shoulder replacements are not intended to withstand activity levels and loads of normal healthy bone, they are a means of restoring mobility and reducing pain for many patients. Component: NA

Reason for recall

Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2011-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.