fda_recall · device_recall · high
ARROW INTERNATIONAL, LLC — Class II recall: FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHET…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:56Z
- Source ID
- Z-1913-2026
- Payload hash
- 9d33bb4d9767d2430b927c5e…
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.