Medline Industries, LP recalled 828 Valve Pack-LF Cannula Kits DYNJ0415366P and DYNJ0415366Q sold nationwide, including California. The cannula catheter may not retain its shape. Stop using the devices immediately and follow recall instructions for refunds or replacements.
The kits contain certain lots of cannula products where the catheter may not retain its shape.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
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Valve Pack-LF Cannula Kits are medical device kits used in clinical settings for IV catheterization.
The catheter may not retain its shape, potentially compromising performance during use in patient care.
This recall is not identified as part of a broader industry pattern.
Hospitals and clinics should screen inventory, halt use of affected units, and coordinate refunds or replacements with Medline.
Recall notices on the FDA enforcement site and Medline’s recall communications; check the kit packaging for model and lot numbers (UDI where available).
Refunds or replacements typically follow the recall process and may take several weeks.
Keep the recall letter and FDA notice; photograph packaging and labels; document lot numbers and where the devices were used.
Model numbers: DYNJ0415366P; DYNJ0415366Q. Where sold: US nationwide distribution, with California noted in the recall notice. When sold: Not specified. Price: Not specified. Quantity: 828 units. Recall date: 2025-08-21. Distribution: US nationwide distribution in California. Manufacturer: Medline Industries, LP. Notes: Lot numbers associated with these models are listed below.
No injuries or incidents have been reported.
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