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DeRoyal Industries Inc Recall 87949

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

DeRoyal Industries Inc Recall 87949 Information

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
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