Stryker Sustainability Solutions Recall
Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Updated April 10, 2026
Stryker Sustainability Solutions is recalling Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER. Hazard: Incomplete seals on sterile product
Is the Stryker Sustainability Solutions recalled? Yes. This product was recalled by FDA on April 10, 2026. Details below.
What is recalled
Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Am I affected
You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.
What to do right now
Voluntary: Firm initiated
The hazard
Incomplete seals on sterile product
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-Z-2195-2026
- Classification
- Class II
- Recalled
- April 10, 2026
Get free recall alerts
New Drugs & Medications recalls, the moment they post.
Free forever. Unsubscribe anytime. We never sell your data.
More Drugs & Medications recalls
ScotchTM Thermal Laminators Recall
ScotchTM Thermal Laminators is recalling 3M Company Recalls ScotchTM Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard. Hazard: The …
Scotch™ Thermal Laminators
The manufacturer Recall
The manufacturer is recalling Regfear Recalls BedsPick Mattresses Due to Risk of Serious Injury or Death from Fire; Violate Mandatory Flammability Standard for …
BedsPick Mattresses
BedsPick Mattresses Recall
BedsPick Mattresses is recalling Regfear Recalls BedsPick Mattresses Due to Risk of Serious Injury or Death from Fire; Violate Mandatory Flammability Standard …
BedsPick Mattresses