Class IIOngoingZ-1439-2026
Olympus Corporation Of The Americas recalls Olympus Resection Inner Sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of…PAMar 4, 2026
2026 device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,237–1,248 of 1,678 recalls
Class IIOngoingZ-1438-2026
Olympus Corporation Of The Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and t…
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of…PAMar 4, 2026
Class IIOngoingZ-1437-2026
Olympus Corporation Of The Americas recalls Olympus Cystoscope Outer Sheath
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.
Olympus Corporation of…PAMar 4, 2026
Class IIOngoingZ-1436-2026
MRIMed Inc. recalls MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved ba…
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
MRIMed Inc.CAMar 4, 2026
Class IIOngoingZ-1435-2026
Medline Industries, LP recalls Meijer STERILE saline wound wash
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.
Medline Industries, LPILMar 4, 2026
Class IIOngoingZ-1434-2026
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT
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.
Medline Industries, LPILMar 4, 2026
Class IIOngoingZ-1433-2026
Medline Industries, LP recalls Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION
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.
Medline Industries, LPILMar 4, 2026
Class IIOngoingZ-1432-2026
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT
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.
Medline Industries, LPILMar 4, 2026
Class IIOngoingZ-1431-2026
Medline Industries, LP recalls Medline Sterile Saline Wound Wash
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.
Medline Industries, LPILMar 4, 2026
Class IIOngoingZ-1430-2026
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha recalls Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR
Software anomaly in the patient positioning system may result in positional discrepancy.
Hitachi, Ltd. Radiatio…Mar 4, 2026
Class IIOngoingZ-1429-2026
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha recalls Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR
Software anomaly in the patient positioning system may result in positional discrepancy.
Hitachi, Ltd. Radiatio…Mar 4, 2026
Class IIOngoingZ-1428-2026
Intuitive Surgical, Inc. recalls Da Vinci 5 ASSY
An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.
Intuitive Surgical, In…CAFeb 25, 2026