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
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-2174-2026
- Classification
- Class II
- Recalled
- April 10, 2026
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