Z-0659-2024 Class II Ongoing
Recall Details
- Product Type
- Devices
- Report Date
- January 17, 2024
- Initiation Date
- December 6, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
Baxter Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM, 1.5-2 MM GLOBAL, c) 7082025: 8CM, 2-2.5 MM GLOBAL, d) 7151015: 15CM, 1-1.5 MM GLOBAL, e) 7151520: 15CM, 1.5- 2 MM GLOBAL, f) 7152025: 15CM, 2- 2.5 MM GLOBAL, g) 7451015: 45CM, 1- 1.5 MM GLOBAL, h) 7451520: 45CM, 1.5- 2 MM GLOBAL, i) 7452025: 45CM, 2- 2.5 MM GLOBAL, j) 7081015ES: 8CM, 1-1.5 MM GLOBAL, k) 7081520ES: 8CM, 1.5- 2 MM GLOBAL, l) 7082025ES: 8CM, 2-2.5 MM GLOBAL, m) 7151015ES: 15CM, 1-1.5 MM GLOBAL, n) 7151520ES: 15CM, 1.5- 2 MM GLOBAL, o) 7152025ES: 15CM, 2-2.5 MM GLOBAL, p) 7451015ES: 45CM, 1-1.5 MM GLOBAL, q) 7451520ES: 45CM, 1.5-2 MM GLOBAL, r) 7452025ES: 45CM, 2-2.5 MM GLOBAL
Reason for Recall
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
Distribution Pattern
US Nationwide distribution.
Code Information
a) 7081015: UDI/DI 0338-9564-17, b) 7081520: UDI/DI 0338-9564-18, c) 7082025: UDI/DI 0338-9564-19, d) 7151015: UDI/DI 0338-9564-12, e) 7151520: UDI/DI 0338-9564-11, f) 7152025: UDI/DI 0338-9564-13, g) 7451015: UDI/DI 0338-9564-14, h) 7451520: UDI/DI 0338-9564-15, i) 7452025: UDI/DI 0338-9564-16, j) 7081015ES: UDI/DI 0338-9564-10, k) 7081520ES: UDI/DI 0338-9564-26, l) 7082025ES: UDI/DI 0338-9564-27, m) 7151015ES: UDI/DI 0338-9564-21, n) 7151520ES: UDI/DI 0338-9564-20, o) 7152025ES: UDI/DI 0338-9564-22, p) 7451015ES: UDI/DI 0338-9564-24, q) 7451520ES: UDI/DI 0338-9564-23, r) 7452025ES: UDI/DI 0338-9564-25, All serial numbers