Product Safety Recalls

Product Recall Tracker

MEDLINE INDUSTRIES, LP – Northfield Recall 94581

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

MEDLINE INDUSTRIES, LP – Northfield Recall 94581 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-2741-2024
Event ID94581
Event DescriptionMedline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H
Product TypeDevices
DistributionWorldwide
Recall ReasonMedical 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.
Device Classification20240904
Device Code InfoDYNJRA2040H, Lot Number 23CBH893; DYNJRA2040H, Lot Number 23HBX547; DYNJRA2040H, Lot Number 23JBN538; DYNJRA2040H, Lot Number 24ABQ696; DYNJRA2040H, Lot Number 24CBG746
Center Classification Date20240828
Recall Initiation Date20240408
Recalling FirmMEDLINE INDUSTRIES, LP - Northfield
Initial Notification Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.