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
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-2177-2026
- Classification
- Class II
- Recalled
- April 10, 2026
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