November 2019 FDA Recall Drug by Oralabs, Incorporated
D-0624-2020 - Cross contamination with other products
This Class II drug recall was voluntarily initiated by Oralabs, Incorporated on November 25, 2019 for the product Drug. The FDA reported the reason for recall as cross contamination with other products. The product was distributed Nationwide and the recall is currently terminated.
Recall Number: D-0624-2020
Cross contamination with other products: undeclared contaminants of phenol and camphor in petroleum jelly tubes.
11-25-2019
12-18-2019
N/A
Recall Profile & Regulatory Data
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
The firm responsible for the recall.
OraLabs, Incorporated
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Method by which the firm first notified the public.
E-Mail
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
Nationwide within the United States
01-27-2021
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
Petroleum jelly (White Petrolatum) USP 100%, packaged in a) 1 oz tube (UPC 1182298884), b) 2.5 oz tube (UPC 1182298541), Distributed by Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011
Batch or Lot Expiration Information
Lot# : a) 44660922 Exp. 09/22; b) 44771122, Exp. 11/22