March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/C
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Mo
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic application
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applicatio
Hazard: Complaints of the ceramic tip of the resection sheath breaking have been received.
March 4, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Hazard: Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
March 4, 2026Medical DevicesFDA
MRIMed Inc. recalls MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with
Hazard: Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM201
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
March 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 FL OZ (21
Hazard: Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.