Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL
Recalling firm: Pharmatech LLC
Why it was recalled
Presence of yeast and potential contamination with B. cepacia.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 2, 2022.
Check your package
Compare the exact product and package details with the label you have.
ProductLeader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628
Package size50 mL
UPC
096295128628FDA code information
All lots remaining within expiry
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 096295128628 | Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628 |
Original FDA recall reason
Presence of yeast and potential contamination with B. cepacia.
Recall details
- Recall number
- F-0627-2018
- Event ID
- 78978
- FDA status
- Terminated
- Initiated
- Aug 16, 2017
- Reported
- Jan 31, 2018
- Classified
- Jan 24, 2018
- Terminated
- Dec 2, 2022
- Quantity
- Unknown
- Location
- Davie, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
MI
FDA source record · F-0627-2018
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.