Medline Industries recalled 828 units of catheter kits on August 21, 2025, due to potential shape retention issues. The affected products include Model Numbers DYNJ0415366P and DYNJ0415366Q. This recall poses a serious risk to patient safety.
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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The recall includes 828 units of VALVE PACK-LF kits with Model Numbers DYNJ0415366P and DYNJ0415366Q. These kits were distributed nationwide, particularly in California.
The catheter in these kits may not retain its shape, which can compromise medical procedures. The hazard classification is Class I, indicating a high risk.
There are no reported incidents or injuries associated with this recall at this time. However, the potential risk to patient safety remains high.
Patients and healthcare providers should stop using these kits immediately. Contact Medline Industries or your healthcare provider for further instructions.
For more information, contact Medline Industries at 1-800-XXXX-XXXX or visit their website at www.medline.com.
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