Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q

FDA device recall Z-2670-2025 · posted 2025-10-01 · Open, Classified

Recall details

Recalling firm

Medline Industries, LP

Reason for recall

The kits contain certain lots of cannula products where the catheter may not retain its shape.

Action taken

An URGENT MEDICAL DEVICE RECALL notification dated 8/21/25 was sent to customers. REQUIRED ACTION: 1.Immediately check your stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. Upon completion of the below actions, please destroy affected product. 2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form. Website link: https://recalls.medline.com. Recall Reference #: R-25-181-FGX1 Recall Code: 3. Your account will receive credit once the response form is submitted. 4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers destroy any affected product. You should include your customers quantities on your response form. If you have any questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.

Root cause

Under Investigation by firm

Status

Open, Classified

Product code

OEZ

Quantity affected

828 units

Distribution

US Nationwide distribution in the state of CA.

Date initiated

2025-08-21

Date posted

2025-10-01

Location

Northfield, IL