fda_recall · device_recall · high
ARROW INTERNATIONAL, LLC — Class II recall: ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)1080…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:56Z
- Source ID
- Z-1911-2026
- Payload hash
- ff7576c3f8d11afcbeb7b904…
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.