Class IIOngoingZ-1442-2026
Olympus Corporation Of The Americas recalls Olympus Resection Sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of…PAMar 4, 2026
Recalls: Under Investigation by firm
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 325–336 of 1,125 recalls
Class IIOngoingZ-1441-2026
Olympus Corporation Of The Americas recalls Olympus Resection Sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of…PAMar 4, 2026
Class IIOngoingZ-1440-2026
Olympus Corporation Of The Americas recalls Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection s…
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of…PAMar 4, 2026
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
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