Covidien, LLC: Medical Device Recall in 2023 - (Recall #: Z-0955-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1

Product Classification:

Class II

Date Initiated: November 23, 2022

Date Posted: January 18, 2023

Recall Number: Z-0955-2023

Event ID: 91318

Reason for Recall:

The product is labeled with the incorrect expiration date.

Status: Ongoing

Product Quantity: 21 units

Code Information:

UDI/DI (GTIN): 10884521825765, Lot Number: 520200

Distribution Pattern:

Foreign Distribution: Hong Kong

Voluntary or Mandated:

Voluntary: Firm initiated