| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111 | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 35cm. Model Number: TB2-0535FC. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112 | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 25cm. Model Number: TB2-0525FC. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-29 | FDA Device | FDA Recall: OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-08 | FDA Device | FDA Recall: Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-08 | FDA Device | FDA Recall: Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser Sy | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutti | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Nu | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Mode | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/C | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar | Olympus Corporation of the Americas | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-11 | FDA Device | FDA Recall: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Gener | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-11 | FDA Device | FDA Recall: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-11 | FDA Device | FDA Recall: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-11 | FDA Device | FDA Recall: Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-11 | FDA Device | FDA Recall: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 h | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-11 | FDA Device | FDA Recall: Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lit | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applicat | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for ur | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological appl | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for uro | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological ap | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A; | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological appli | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applica | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in u | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological appl | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological appli | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications. | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applicat | Olympus Corporation of the Americas | Class II | N/A |
| 2026-03-04 | FDA Device | FDA Recall: Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for | Olympus Corporation of the Americas | Class II | N/A |