Class IIOngoingZ-1458-2026
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT
Knee and Humeral socket implants contain incorrect labeling.
Encore Medical, LPTXMar 4, 2026
Recalls in Texas
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 87 recalls
Class IIOngoingZ-1234-2026
Encore Medical, LP recalls EMPOWR Acetabular System: Liner
942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay t…
Encore Medical, LPTXFeb 11, 2026
Class IIOngoingZ-1233-2026
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert 5R 14MM
942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay t…
- Polymer/Metal/Polymer Cemented Semi-Constrained Patellofemorotibial Knee Prosthesis
- Labeling Change Control
Encore Medical, LPTXFeb 11, 2026
Class IOngoingZ-0939-2026
Alcon Research LLC recalls Brand Name: Alcon Laboratories
Ophthalmic procedure packs may have incomplete seals affecting sterility.
Alcon Research LLCTXDec 31, 2025
Class IIOngoingZ-0961-2026
Abbott Laboratories recalls Alinity ci-series System Control Module (SCM)
Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction.…
Abbott LaboratoriesTXDec 24, 2025
Class IIIOngoingZ-0896-2026
Orthofix U.S. LLC recalls Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer Sys…
Labeling contains claims that are not consistently present.
Orthofix U.S. LLCTXDec 17, 2025
Class IIIOngoingZ-0895-2026
Orthofix U.S. LLC recalls Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catal…
Labeling contains claims that are not consistently present.
Orthofix U.S. LLCTXDec 17, 2025
Class IIIOngoingZ-0894-2026
Orthofix U.S. LLC recalls Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model…
Labeling contains claims that are not consistently present.
Orthofix U.S. LLCTXDec 17, 2025
Class IIIOngoingZ-0893-2026
Orthofix U.S. LLC recalls Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System M…
Labeling contains claims that are not consistently present.
Orthofix U.S. LLCTXDec 17, 2025
Class IIIOngoingZ-0892-2026
Orthofix U.S. LLC recalls Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Cat…
Labeling contains claims that are not consistently present.
Orthofix U.S. LLCTXDec 17, 2025
Class IIIOngoingZ-0891-2026
Orthofix U.S. LLC recalls Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer S…
Labeling contains claims that are not consistently present.
Orthofix U.S. LLCTXDec 17, 2025
Class IIOngoingZ-0589-2026
Argon Medical Devices, Inc recalls Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 Th…
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is appl…
Argon Medical Devices,…TXDec 3, 2025