Arrow International Inc recalls Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

Recalled January 29, 2020 · FDA recall Z-0837-2020 · Arrow International

Hazard

Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH. · FDA Class II

Units

575

Sold at

US: FL

Description

Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.

Product

Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

Manufacturer(s)

Arrow International Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →