| Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Prod recall (Z-1290-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530 Prod recall (Z-1291-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030 Prod recall (Z-1292-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple Lumen S recall (Z-1293-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0725 Pr recall (Z-1294-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020 Prod recall (Z-1295-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025 Prod recall (Z-1296-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Numbe recall (Z-1297-2026) | Olympus Corporation of the Americas | 2026-02-05 |
| Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single Use Electrosurgi recall (Z-1222-2026) | Olympus Corporation of the Americas | 2026-01-30 |
| Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus Single Use Elect recall (Z-1223-2026) | Olympus Corporation of the Americas | 2026-01-30 |
| Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Numb recall (Z-0570-2026) | Olympus Corporation of the Americas | 2025-11-25 |
| Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V Model/Catalog recall (Z-0579-2026) | Olympus Corporation of the Americas | 2025-11-21 |
| Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product Name: O recall (Z-0572-2026) | Olympus Corporation of the Americas | 2025-11-20 |
| Brand Name: Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer Model recall (Z-0452-2026) | Olympus Corporation of the Americas | 2025-11-07 |
| Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Elect recall (Z-0482-2026) | Olympus Corporation of the Americas | 2025-11-07 |
| Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Singl recall (Z-0483-2026) | Olympus Corporation of the Americas | 2025-11-07 |
| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 recall (Z-0045-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 recall (Z-0046-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 recall (Z-0047-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 recall (Z-0048-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 recall (Z-0049-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 recall (Z-0050-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180 recall (Z-0051-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 recall (Z-0052-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 recall (Z-0053-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 recall (Z-0054-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 recall (Z-0055-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 recall (Z-0056-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 recall (Z-0057-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 recall (Z-0058-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 recall (Z-0059-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 recall (Z-0060-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180 recall (Z-0061-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC recall (Z-0062-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 recall (Z-0063-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 recall (Z-0064-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 recall (Z-0065-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 recall (Z-0066-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 recall (Z-0067-2026) | Olympus Corporation of the Americas | 2025-10-16 |
| ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019. The ViziShot 2 recall (Z-2484-2025) | Olympus Corporation of the Americas | 2025-09-05 |
| Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-41 recall (Z-2338-2025) | Olympus Corporation of the Americas | 2025-08-19 |
| Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-41 recall (Z-2339-2025) | Olympus Corporation of the Americas | 2025-08-19 |
| Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silic recall (Z-2139-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. recall (Z-2140-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter ac recall (Z-2141-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator a recall (Z-2142-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compat recall (Z-2143-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Ellik Latex Bulb, Ellik Evacuator. Model Number: 194-2. The Ellik Evacuator and adapter ac recall (Z-2144-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Ellik Evacuator Adapter, Locking. Model Number: 190-NRS. The Ellik Evacuator and adapter a recall (Z-2145-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Cone with Male Tubing, Non-Locking, Ellik Evacuator. Model Number: 191-NRS. The Ellik Evac recall (Z-2146-2025) | Olympus Corporation of the Americas | 2025-07-21 |
| Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser recall (Z-1920-2025) | Olympus Corporation of the Americas | 2025-06-06 |
| Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed La recall (Z-1921-2025) | Olympus Corporation of the Americas | 2025-06-06 |
| Brand Name: Powered Laser Surgical Instrument Product Name: Soltive SuperPulsed Laser Fibe recall (Z-1922-2025) | Olympus Corporation of the Americas | 2025-06-06 |
| Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable Laser Fibers recall (Z-1923-2025) | Olympus Corporation of the Americas | 2025-06-06 |
| Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V recall (Z-1911-2025) | Olympus Corporation of the Americas | 2025-06-05 |
| Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser recall (Z-1715-2025) | Olympus Corporation of the Americas | 2025-05-01 |
| Olympus Single Use Guide Sheath Kits with the following product descriptions and model num recall (Z-1071-2025) | Olympus Corporation of the Americas | 2025-02-11 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0993-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0994-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0995-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0996-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0997-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0998-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-0999-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-1000-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-1001-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-1002-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: T recall (Z-1003-2025) | Olympus Corporation of the Americas | 2025-01-21 |
| Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog Number: MAJ-891. Th recall (Z-0905-2025) | Olympus Corporation of the Americas | 2025-01-16 |
| LithoCrushV Single Use Mechanical Lithotriptor V. Model Number: BML-V442QR-30. Single Use recall (Z-0962-2025) | Olympus Corporation of the Americas | 2025-01-16 |
| Duravent Silicone Ventilation Tube. Model Number: 240075. recall (Z-0707-2025) | Olympus Corporation of the Americas | 2024-12-19 |
| EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190 recall (Z-0620-2025) | Olympus Corporation of the Americas | 2024-12-05 |
| Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product Name: Olympus GI recall (Z-0498-2025) | Olympus Corporation of the Americas | 2024-11-20 |
| Brand Name: UroPass Ureteral Access Sheaths Product Name: Ureteral Access Sheaths Model/Ca recall (Z-0364-2025) | Olympus Corporation of the Americas | 2024-11-12 |
| Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A S recall (Z-0351-2025) | Olympus Corporation of the Americas | 2024-11-08 |
| Olympus Electrosurgical Generator, Model Number ESG-410 (SEP) Version WA91327U recall (Z-0264-2025) | Olympus Corporation of the Americas | 2024-10-30 |
| EZDilate Wire Guided Balloon- Indicated for use in adult and adolescent (> 12 years) popul recall (Z-0225-2025) | Olympus Corporation of the Americas | 2024-10-25 |
| Olympus Endoscopic Flushing Pump, Model/Catalog Number: OFP-2 (K10001141) recall (Z-0229-2025) | Olympus Corporation of the Americas | 2024-10-25 |
| Quest Spectrum 3 Fluorescent Imaging System Model/Catalog Number: ART-SYS-0029, ART-SYS-00 recall (Z-0232-2025) | Olympus Corporation of the Americas | 2024-10-25 |
| Olympus Gastrointestinal Videoscope, Model/Catalog Number: GIF-1100 recall (Z-0181-2025) | Olympus Corporation of the Americas | 2024-10-23 |
| Soltive Premium SuperPulsed Laser - Intended for incision, excision, resection, ablation, recall (Z-0134-2025) | Olympus Corporation of the Americas | 2024-10-18 |
| Soltive Pro SuperPulsed Laser Systems-Intended for incision, excision, resection, ablation recall (Z-0135-2025) | Olympus Corporation of the Americas | 2024-10-18 |
| EVIS EXERA III Video System Center Model Number CV-190. Intended to be used with OLYMPUS c recall (Z-0056-2025) | Olympus Corporation of the Americas | 2024-10-11 |
| Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus endoscopes and electr recall (Z-1547-2024) | Olympus Corporation of the Americas | 2024-09-12 |
| Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus endoscopes and electr recall (Z-1548-2024) | Olympus Corporation of the Americas | 2024-09-12 |
| The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cann recall (Z-2540-2024) | Olympus Corporation of the Americas | 2024-08-08 |
| The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cann recall (Z-2541-2024) | Olympus Corporation of the Americas | 2024-08-08 |
| The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cann recall (Z-2542-2024) | Olympus Corporation of the Americas | 2024-08-08 |
| Soltive Premium SuperPulsed Laser System, Model TFL-PLS recall (Z-2504-2024) | Olympus Corporation of the Americas | 2024-08-05 |
| Soltive Pro SuperPulsed Laser System, Model TFL-SLS recall (Z-2505-2024) | Olympus Corporation of the Americas | 2024-08-05 |
| Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL recall (Z-2506-2024) | Olympus Corporation of the Americas | 2024-08-05 |
| ESG-410 Electrosurgical Generator- In conjunction with electrosurgical accessories intende recall (Z-2415-2024) | Olympus Corporation of the Americas | 2024-07-23 |
| EasySuite 4K Integrated Operating Room System Model/Catalog Number: EasySuite 4K- The Easy recall (Z-2233-2024) | Olympus Corporation of the Americas | 2024-06-28 |
| OES 4000 Hysteroscope, Model/Catalog Number: A4674A recall (Z-2029-2024) | Olympus Corporation of the Americas | 2024-06-06 |
| InstaClear Lens Sheath. The InstaClear lens cleaner system and versatile sheath cleans and recall (Z-1888-2024) | Olympus Corporation of the Americas | 2024-05-23 |
| POWERSEAL 5 mm, 23 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use i recall (Z-1699-2024) | Olympus Corporation of the Americas | 2024-04-30 |
| POWERSEAL 5 mm, 37 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use i recall (Z-1700-2024) | Olympus Corporation of the Americas | 2024-04-30 |
| POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use i recall (Z-1701-2024) | Olympus Corporation of the Americas | 2024-04-30 |
| Hemostasis Probe, Model: CD-B622LA recall (Z-1481-2024) | Olympus Corporation of the Americas | 2024-04-05 |
| SOLTIVE Pro SuperPulsed Laser (TFL-SLS ) recall (Z-1384-2024) | Olympus Corporation of the Americas | 2024-03-27 |