Why it was recalled
Microbial contamination
Product description
NET Remedies #9 ER 911 Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4209-2
Lot numbers, UPCs & expiration codes
Lots: NR-071118A Exp. 07/20; NR-071218A Exp. 07/20; NR-071218C Exp. 07/20; NR-081017M Exp. 08/19; NR-110117H Exp. 11/19; NR-020118K Exp. 02/20; NR-111517C Exp. 11/19; NR-120317J Exp. 12/19
Where it was sold
U.S.A. Nationwide, Canada, and Australia.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0958-2019
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Jul 20, 2018
- FDA report date
- Mar 20, 2019
- Quantity
- 20098 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- King Bio Inc.
Original FDA data
Every field from FDA enforcement report D-0958-2019, exactly as published.
Show all FDA fields
- City
- Asheville
- State
- NC
- Status
- Terminated
- Country
- United States
- Event ID
- 80601
- Address
- 3 Westside Dr
- Code information
- Lots: NR-071118A Exp. 07/20; NR-071218A Exp. 07/20; NR-071218C Exp. 07/20; NR-081017M Exp. 08/19; NR-110117H Exp. 11/19; NR-020118K Exp. 02/20; NR-111517C Exp. 11/19; NR-120317J Exp. 12/19
- Postal code
- 28806-2846
- Report date
- Mar 20, 2019
- Product type
- Drugs
- Recall number
- D-0958-2019
- Classification
- Class I
- Recalling firm
- King Bio Inc.
- Product quantity
- 20098 bottles
- Termination date
- Jan 19, 2022
- Reason for recall
- Microbial contamination
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- NET Remedies #9 ER 911 Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4209-2
- Distribution pattern
- U.S.A. Nationwide, Canada, and Australia.
- Recall initiation date
- Jul 20, 2018
- Initial firm notification
- Press Release
- Center classification date
- Mar 8, 2019