Product Safety Recalls

Product Recall Tracker

DeRoyal Industries Inc Recall 87949

Description: DeRoyal Angio Cath Removal Tray, REF 89-9936.02

DeRoyal Industries Inc Recall 87949 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1834-2021
Event ID87949
Event DescriptionDeRoyal Angio Cath Removal Tray, REF 89-9936.02
Product TypeDevices
DistributionUS Nationwide distribution to the states of MS, VA, LA, and NY.
Quantity60 trays
Recall ReasonDeRoyal manufactured certain lots of surgical procedure pack products using Hospira Pfizer 1% Lidocaine which was subsequently recalled due to mislabeling; the product is 0.5% Bupivacaine
Device Classification20210616
Device Code InfoLot Numbers: 54368716, exp. 6/01/2022
Center Classification Date20210610
Recall Initiation Date20210514
Recalling FirmDeRoyal Industries Inc
Initial Notification E-Mail
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.