Reported May 20, 2026 · Ongoing
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Stryker Sustainability Solutions
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Sustainability Solutions · 1810 W Drake Dr · Tempe, AZ · 85283-4327
Is this the product you have?
- BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI 00885825003869
- Lot Numbers
83 of 83 codes
397523542537854277547429745946560954818154497226640658154253786427754842974604656096481815550323904180953425379142969754363237471762348181565032392422397342549184296977440442747176244831929503239342537734254919429697844811364717625483193150323944253774425492142969794494845474201548366455032395425377542549224296980454247547420174836646503271042537784254923429698145445864742018485870850558554253779427754142969824545898
- Amount recalled
- 90 units
This recall covers 26 products
The agency filed one notice per product. You are reading one of them; the other 25 are below.
13 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Incomplete seals on sterile product
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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