FDA Device recall Z-0108-2024
THUNDERBEAT, 5MM, 35CM, Front-actuated Grip Type S. Model: TB-0535FCS Indicated for open, laparoscopic (including single-site surgery) gene…
- FDA Device
- Class II
- ongoing
- Published 2023-10-18
On 2023-10-18 the FDA classified a Class II recall of THUNDERBEAT, 5MM, 35CM, Front-actuated Grip Type S. Model: TB-0535FCS Indicated for open, laparoscopic (including single-site surgery) gene… by Olympus, citing thunderbeats blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position may result in prolonged surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0108-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-12 |
| Published | 2023-10-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
THUNDERBEAT, 5MM, 35CM, Front-actuated Grip Type S. Model: TB-0535FCS Indicated for open, laparoscopic (including single-site surgery) general surgery and gynecological surgery (including urologic, thoracic, plastic and reconstructive, bowel resections, cholecystectomies, Nissen fundoplication, adhesiolysis, oophorectomy, hysterectomies (both vaginal assisted and abdominal) etc) and endoscopic surgery or in any procedure in which cutting, vessel ligation (sealing and cutting), coagulation, grasping, and dissection is performed
Reason
Thunderbeats blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position may result in prolonged surgery
Identifiers
| code_info | UDI-DI: 4953170409677 Lot Numbers: KR271978 KR314612 KR314613 KR314615 KR314617 KR314618 KR314619 KR314621 KR31…UDI-DI: 4953170409677 Lot Numbers: KR271978 KR314612 KR314613 KR314615 KR314617 KR314618 KR314619 KR314621 KR314622 KR314623 KR314624 KR314626 KR314627 KR314628 KR314629 KR314630 KR314631 KR314632 KR314633 KR314634 KR314638 KR314640 KR314641 KR314644 KR314647 KR314648 KR314650 KR314651 KR314652 KR314654 KR314655 KR314657 KR314659 KR314660 KR314662 KR314663 KR314668 KR314670 KR314671 KR314672 KR314673 KR314674 KR314675 KR314676 KR314679 KR316617 KR316627 KR316629 KR316637 KR316683 KR319616 KR319643 KR319655 KR332609 KR332615 KR332616 KR332623 KR332626 KR335733 KR335754 KR335760 KR335769 KR335770 KR335776 KR335781 KR335784 KR335785 KR335794 KR335796 KR335836 PW308606 PW308607 PW308609 PW308611 PW308613 PW308615 PW308616 PW308663 PW308772 PW308773 PW308774 PW308775 PW308776 PW308786 PW308788 Lots Added January 11, 2024: KR271978 KR314619 KR314627 KR314633 KR314648 KR335770 KR310806 KR314612 KR314621 KR314628 KR314634 KR332616 KR |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0108-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.