Boston Scientific: Medical Device Recall in 2020 - (Recall #: Z-1735-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: M006175272080 (edited 1/13/2021)

Product Classification:

Class II

Date Initiated: March 9, 2020

Date Posted: April 29, 2020

Recall Number: Z-1735-2020

Event ID: 85227

Reason for Recall:

An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device

Status: Ongoing

Product Quantity: 5 units

Code Information:

Lot Number: 24958079 (edited 1/13/2021)

Distribution Pattern:

Nationwide Foreign: Europe, Middle East and Africa, the Americas (North America and South America, Asia Pacific and Japan

Voluntary or Mandated:

Voluntary: Firm initiated