Surgical Tools and Cardiovascular Specialty marketing recall
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004…
Why was Surgical Tools and Cardiovascular Specialty marketing recalled?
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).
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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 00085412532622; w) 60400BIOS, UDI/DI 00085412532547; x) 60450BIOS, UDI/DI 00085412532639
- Product
- Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004…
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 83971 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, Ireland, United Kingdom, and Hong Kong.
- Recall date
- April 24, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)