FDA Device recall Z-1522-2024
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-21…
- FDA Device
- Class II
- ongoing
- Published 2024-04-24
On 2024-04-24 the FDA classified a Class II recall of Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-21… by Baxter Healthcare, citing the Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1522-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-22 |
| Published | 2024-04-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure US version which affect: Flo-Rester Disposable Internal Vessel Occluder, Item Numbers: a) 50100, b) 50125, c) 50150, d) 50175, e) 50200, f) 50225, g) 50250, h) 50275, i) 50300, j) 50350, k) 50400, l) 50450BIOS, m) 60100, n) 60125BIOS, o) 60150BIOS, p) 60175, q) 60200BIOS, r) 60225BIOS, s) 60250BIOS, t) 60275, u) 60300, v) 60350, w) 60400BIOS, x) 60450BIOS
Reason
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Identifiers
| code_info | Cardiovascular Specialty marketing brochures: Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-…Cardiovascular Specialty marketing brochures: Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure US version Flo-Rester: ALL SERIAL NUMBERS: a) 50100, UDI/DI 00085412532592; b) 50125, UDI/DI 00085412532684; c) 50150, UDI/DI 00085412532608; d) 50175, UDI/DI 00085412532691; e) 50200, UDI/DI 00085412532431; f) 50225, UDI/DI 00085412532448; g) 50250, UDI/DI 00085412532455; h) 50275, UDI/DI 00085412532462; i) 50300, UDI/DI 00085412532479; j) 50350, UDI/DI 00085412532486; k) 50400, UDI/DI 00085412532493; l) 50450BIOS, UDI/DI 00085412532509; m) 60100, UDI/DI 00085412532516; n) 60125BIOS, UDI/DI 00085412532110; o) 60150BIOS, UDI/DI 00085412532127; p) 60175, UDI/DI 00085412532134; q) 60200BIOS, UDI/DI 00085412532141; r) 60225BIOS, UDI/DI 00085412532158; s) 60250BIOS, UDI/DI 00085412532523; t) 60275, UDI/DI 00085412532615; u) 60300, UDI/DI 00085412532530; v) 60350, UDI/DI 00085 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1522-2024%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.