fda_recall · device_recall · high
Medline Industries, LP — Class II recall: Medline Kits: 1) ENT PACK, Model Number: DYNJ59030B; 2) ENT, Model Number: DY…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:55Z
- Source ID
- Z-1839-2026
- Payload hash
- ac67335a339d404793c2bec8…
Summary
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.