Arrow International Inc recalls Percutaneous Sheath Introducer Kit with Integral Hemostasis
Recalled Product
Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7.5 - 8 Fr. Catheters; Product Code: ASK-09903-UPA
Hazard / Issue
Product sterility may be compromised due to unsealed packaging.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot Numbers: 13F17E0762 13F17F0599 13F17H0058 13F17J0241 13F17L0114 13F17L0485
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime