FDA Devices Moderate Class II Ongoing

MEDLINE OPEN HEART, REF DYNJ904261B

Reported: October 23, 2024 Initiated: August 28, 2024 #Z-0122-2025

Product Description

Reason for Recall

Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.

Details

Recalling Firm: MEDLINE INDUSTRIES, LP - Northfield
Units Affected: 30 units
Distribution: US Nationwide distribution.
Location: Northfield, IL

Frequently Asked Questions

What product was recalled? ▼

MEDLINE OPEN HEART, REF DYNJ904261B. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 30 units.

Why was this product recalled? ▼

Which agency issued this recall? ▼

This recall was issued by the FDA Devices on October 23, 2024. Severity: Moderate. Recall number: Z-0122-2025.

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