RecalledThisWeek Search
Medium risk Medical DevicesClass II

BARD Dynamic Tip Steerable Recall

BARD Dynamic Tip Steerable, Product Number 6DYNTP001;

Updated April 10, 2026

The BARD Dynamic Tip Steerable medical device (Product Number 6DYNTP001) has incomplete seals on its sterile packaging, which could allow contamination. The manufacturer has voluntarily recalled this product.

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

What is recalled

BARD Dynamic Tip Steerable, Product Number 6DYNTP001, manufactured by Stryker Sustainability Solutions.

Am I affected

You are affected if you have the BARD Dynamic Tip Steerable with Product Number 6DYNTP001. Check the product label or packaging for this exact model number.

What to do right now

Stop using this product immediately. Contact your healthcare provider or hospital to determine whether you have received this device and what steps to take next, as it may have been used in a medical procedure.

The hazard

Incomplete seals on sterile product

Brands affected

Stryker Sustainability Solutions
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2177-2026
Classification
Class II
Recalled
April 10, 2026
Read the official notice

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