PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H

Reported: September 4, 2024 Initiated: April 8, 2024 #Z-2741-2024

Product Description

Medline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H

Reason for Recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Details

Distribution
Worldwide
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H. Recalled by MEDLINE INDUSTRIES, LP - Northfield.
Why was this product recalled?
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 4, 2024. Severity: Moderate. Recall number: Z-2741-2024.