RecalledThisWeek Search
High risk Medical DevicesClass II

BARD Dynamic Deca Steerable Recall

BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Updated April 10, 2026

BARD Dynamic Deca Steerable electrophysiology catheters (Product Number 201101) have incomplete seals on their sterile packaging, which could allow contamination. These reprocessed medical devices are used during heart procedures and require sterility to be safe.

Is the Stryker Sustainability Solutions recalled? Yes. This product was recalled by FDA on April 10, 2026. Details below.

What is recalled

BARD Dynamic Deca Steerable, Product Number 201101 (reprocessed electrophysiology catheter). Check your product label for this exact product number.

Am I affected

You are affected if you have or use a BARD Dynamic Deca Steerable catheter with Product Number 201101.

What to do right now

Stop using this device immediately. Contact Stryker Sustainability Solutions or your healthcare provider right away for guidance on replacement or safe handling of this product.

The hazard

Incomplete seals on sterile product

Brands affected

Stryker Sustainability Solutions
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2174-2026
Classification
Class II
Recalled
April 10, 2026
Read the official notice

Get free recall alerts

New Medical Devices recalls, the moment they post.

Free forever. Unsubscribe anytime. We never sell your data.

More Medical Devices recalls