fda_recall · device_recall · high
ARROW INTERNATIONAL, LLC — Class II recall: PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:57Z
- Source ID
- Z-1912-2026
- Payload hash
- fb4bd66cef0514ee3c9bffcd…
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.