Medline Valve Pack (Unknown) – Catheter Shape Retention (2025)
Catheter shape retention issue may require product inspection.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q
Lot Codes / Batch Numbers
1) DYNJ0415366P, UDI-DI: 10195327177966(each), 40195327177967(case), Lot Number: 24DMG366, 2) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25EMD672, 3) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25GMD016, 4) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25AMB610, 5) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25BMJ241, 6) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25CMI425, 7) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24DMC189, 8) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24EMC463, 9) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24GMJ353, 10) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24IMB824, 11) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24KME116
Products Sold
1) DYNJ0415366P, UDI-DI: 10195327177966(each), 40195327177967(case), Lot Number: 24DMG366; 2) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25EMD672; 3) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25GMD016; 4) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25AMB610; 5) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25BMJ241; 6) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 25CMI425; 7) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24DMC189; 8) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24EMC463; 9) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24GMJ353; 10) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24IMB824; 11) DYNJ0415366Q, UDI-DI: 10195327678227(each), 40195327678228(case), Lot Number: 24KME116
A medical device manufacturer is recalling Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ041 due to The kits contain certain lots of cannula products where the catheter may not retain its shape.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The kits contain certain lots of cannula products where the catheter may not retain its shape.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026