Medtronic Inc.: Medical Device Recall in 2024 - (Recall #: Z-0623-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.

Product Classification:

Class II

Date Initiated: November 20, 2023

Date Posted: January 10, 2024

Recall Number: Z-0623-2024

Event ID: 93558

Reason for Recall:

Seal defects could compromise the ability of the product packaging to maintain sterility.

Status: Completed

Product Quantity: 1

Code Information:

Lot number B644679, UDI-DI 00643169728974.

Distribution Pattern:

US Nationwide distribution in the state of MN.

Voluntary or Mandated:

Voluntary: Firm initiated