BARD Dynamic XT Steerable recall
BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Why was BARD Dynamic XT Steerable recalled?
Incomplete seals on sterile product
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI 00885825003890, Lot Numbers: 4064760, 4336810, 4381356, 4381359, 4401919.
- Product
- BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Recalling firm
- Stryker Sustainability Solutions
- Quantity
- 5 units
- Distribution
- US Nationwide and the countries of Israel and Canada.
- Recall date
- May 20, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)