HIGH
FDA DEVICE
BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
Stryker Sustainability Solutions
Incomplete seals
Stryker Sustainability Solutions Recalls
27 recalls found for Stryker Sustainability Solutions. Check if any of your products are affected.
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
Stryker Sustainability Solutions recalled 56,740 color cuff tourniquet cuffs due to potential detachment from the bladder. The recall affects 18" and 24" cuffs across multiple U.S. states. Patients and healthcare providers should stop using these devices immediately and follow manufacturer instructions.
Stryker Sustainability Solutions
Due to
Brand Statistics
Total Recalls
27
Pages
2