Skip to content
Recall Observatory FDA recall evidence

Device product

DeRoyal Angio Cath Removal Tray, REF 89-9936.02

Z-1834-2021

May 14, 2021

Class I

Product summary

Firm
DeRoyal Industries Inc
Event
Event 87949
Status
Terminated
Classification
Class I
Quantity
60 trays
Official record key
device-enforcement:Z-1834-2021

Official wording

Reason: DeRoyal 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

Code information: Lot Numbers: 54368716, exp. 6/01/2022

Distribution pattern: US Nationwide distribution to the states of MS, VA, LA, and NY.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    mislabeling