Class IIOngoingZ-1460-2026
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKE…
Knee and Humeral socket implants contain incorrect labeling.
Encore Medical, LPTXMar 4, 2026
Recalls: Process control
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 205–216 of 816 recalls
Class IIOngoingZ-1459-2026
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS
Knee and Humeral socket implants contain incorrect labeling.
Encore Medical, LPTXMar 4, 2026
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
Class IIOngoingZ-1426-2026
Centinel Spine, Inc. recalls Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software…
Products were mislabeled as the 6mm product but included the 5 mm product.
Centinel Spine, Inc.PAFeb 25, 2026
Class IIOngoingZ-1367-2026
Bard Peripheral Vascular Inc recalls Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff…
Due to damage to outer tray that can potentially compromise the sterile barrier
Bard Peripheral Vascul…AZFeb 25, 2026
Class IIOngoingZ-1366-2026
Medline Industries, LP recalls Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may r…
Medline Industries, LPILFeb 25, 2026
Class IIOngoingZ-1361-2026
Steris Corporation recalls Barco MNA with the HexaVue IP Integration System
This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.
Steris CorporationOHFeb 18, 2026
Class IIOngoingZ-1299-2026
FUJIFILM Healthcare Americas Corporation recalls FDR Visionary Suite
It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue to be supplied to the power supply circuit even if…
FUJIFILM Healthcare Am…MAFeb 11, 2026
Class IIOngoingZ-1297-2026
Olympus Corporation Of The Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog N…
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of…PAFeb 11, 2026
Class IIOngoingZ-1296-2026
Olympus Corporation Of The Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025…
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of…PAFeb 11, 2026
Class IIOngoingZ-1295-2026
Olympus Corporation Of The Americas recalls Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020…
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of…PAFeb 11, 2026
Class IIOngoingZ-1294-2026
Olympus Corporation Of The Americas recalls Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-072…
Devices which did not undergo thermoforming could deform and lose performance.
Olympus Corporation of…PAFeb 11, 2026