fda_recall · device_recall · high
Medline Industries, LP — Class II recall: Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:53Z
- Source ID
- Z-1834-2026
- Payload hash
- b93619d24e644e550dee3cc8…
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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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.