Recall Z-2670-2025— Medline Industries, LP
Class I · Ongoing
Class I FDA medical device recall by Medline Industries, LP, initiated 2025-08-21. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q. Reason: The kits contain certain lots of cannula products where the catheter may not retain its shape..
- Recalling firm
- Medline Industries, LP
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2025-08-21
- Firm location
- Northfield, IL, United States
Product description
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q
Reason for recall
The kits contain certain lots of cannula products where the catheter may not retain its shape.
Data sourced from openFDA. This site is unofficial and independent of the FDA.