fda_recall · device_recall · critical
ARROW INTERNATIONAL, LLC — Class I recall: Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1; EPIDURAL…
- Event date
- 2026-06-24 00:00:00Z
- Observed
- 2026-07-09 22:51:58Z
- Source ID
- Z-2371-2026
- Payload hash
- 1b73b7b0eb00a8e625fec29a…
Summary
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to seri… Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.