September 2017 FDA Recall Drug by Deserving Health International Corp
D-0011-2018 - Lack of Assurance of Sterility
This Class II drug recall was voluntarily initiated by Deserving Health International Corp on September 20, 2017 for the product Drug. The FDA reported the reason for recall as lack of assurance of sterility. The product was distributed in Product was distributed throughout the United States. and the recall is currently terminated.
Recall Number: D-0011-2018
Lack of Assurance of Sterility
09-20-2017
10-25-2017
623 dropper bottles
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.
Deserving Health International Corp
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.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
Product was distributed throughout the United States.
01-24-2019
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
Symbio Muc Eye, 0.17 fl.oz. 5mL bottles, Manufactured for and distributed in the US b: Biological Health Group Corp. Bremerton, WA 98337. NDC 69711-125-61
Batch or Lot Expiration Information
Lot# : DM17B12, Exp 03/2020; DM16L44, Exp 12/2019; DM16L07, Exp12/2019