FDA-Device2016-09-21Class II
Catheter, Intravascular, Therapeutic, Long Term Greater than 30 days. An access kit only, contains no base components
Arrow International Inc
Hazard
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.
Sold states
US Distribution to states of: NC, OH, FL, and MD.
Affected count
6,121 units in total
Manufactured in
2400 Bernville Rd, N/A, Reading, PA, United States
Products
Catheter, Intravascular, Therapeutic, Long Term Greater than 30 days. An access kit only, contains no base components
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2771-2016Don't want to check this manually?
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