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Recall Observatory FDA recall evidence

Device product

DeRoyal Ultra/Mammo Tray, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) swab, for preparation of the patient skin prior to surgery or injection.

Z-0879-2022

March 03, 2022

Class II

Product summary

Firm
DeRoyal Industries Inc
Event
Event 89737
Status
Terminated
Classification
Class II
Quantity
780 kits
Official record key
device-enforcement:Z-0879-2022

Official wording

Reason: A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.

Code information: SKU/Part Number 89-4990.06; UDI 00749756623599 Lot Numbers (Expiration Date): Lot 53334442 (exp 05/01/2021), Lot 53815781 (exp 06/01/2022), Lot 54685720 (exp 06/01/2022), Lot 55247529 (exp 03/01/2023), Lot 55967067 (exp 04/01/2023)

Distribution pattern: US distribution to Florida, New Jersey, and Tennessee

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.

Field note

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