Medline Convenience Kits: NEURO LAMINECTOMY-LF, Model Number: DYNJ53799 - Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilizat

Source: FDA | Recall date: 05/13/2026

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Start Free Recall Tracking How Recall Alerts Work

Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.

Affected product: Medline Convenience Kits: NEURO LAMINECTOMY-LF, Model Number: DYNJ53799

Summary: Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility as

Hazard: Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility as

Open Official Recall Notice Back to Home

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Start Free Recall Tracking How Recall Alerts Work

Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.