HIGH
FDA DEVICE
BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
Brand hub
Stryker Sustainability Solutions Recalls
27 recalls found for Stryker Sustainability Solutions. Check current safety alerts and related brands before using affected products.
- Active recalls
- 27
- Pages
- 2
HIGH
FDA DEVICE
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
HIGH
FDA DEVICE
Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
HIGH
FDA DEVICE
Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
HIGH
FDA DEVICE
Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
HIGH
FDA DEVICE
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
Health & Personal Care
HIGH
FDA DEVICE
Stryker Sustainability Solutions Color Cuff Recall Expands to 56,740 Cuffs Over Detachment Risk (202
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
Stryker Sustainability Solutions
Due to
Brand Statistics
Total Recalls
27
Pages
2