fda_recall · device_recall · high
ARROW INTERNATIONAL, LLC — Class II recall: ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS C…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:56Z
- Source ID
- Z-1914-2026
- Payload hash
- 1ab36ed92adc71e89e516833…
Summary
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.