FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major Certa-Vite Liquid 236 mL UPC 00904-5023-09
- Published
- January 31, 2018
- Distribution
- MI
Pharmatech LLC Recall: Presence of yeast and potential contamination with B. cepacia.
United States
TerminatedClass II
- Company
- Pharmatech LLC
- Product
- Leader Liquid Vitamin D Supplement for Breastfed Infants 400…
- Recall date
- August 16, 2017
- Terminated
- December 2, 2022
- Source
- FDA
Reason for recall
Presence of yeast and potential contamination with B. cepacia.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628 | 096295128628 | Unknown | All lots remaining within expiry |
Distribution
- MI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0627-2018
- Event ID
- 78978
- Status
- Terminated
- Classification
- Class II
- Company
- Pharmatech LLC
- Product description
- Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628
- Quantity
- Unknown
- Reason
- Presence of yeast and potential contamination with B. cepacia.
- Recall initiation date
- August 16, 2017
- Report date
- January 31, 2018
- Classification date
- Not published in this source record
- Termination date
- December 2, 2022
- Distribution pattern
- MI
- UPC, lot, and code information
- UPC 096295128628; All lots remaining within expiry
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78978 with 9 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Leader Liquid Multivitamin Supplement for Infants and Toddle…
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major Poly-Vita Drops w/ Iron 50 mL UPC 00904-5100-50
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major Tri-Vita Drops 50 mL UPC 00904-6274-50
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Tri-Vitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-850…
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major Poly-Vita Drops 50 mL UPC 00904-5099-50
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Polyvitamin Liquid 1 2/3 fl. oz. (50 mL) UPC 00536-845…
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major D-Vita Drops 50 mL UPC 00904-6273-50
- Published
- January 31, 2018
- Distribution
- MI
Responsible company: Pharmatech LLC
Other recalls from Pharmatech LLC
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Major Certa-Vite Liquid 236 mL UPC 00904-5023-09
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Leader Liquid Multivitamin Supplement for Infants and Toddle…
- Published
- January 31, 2018
- Distribution
- MI
FDA Recall United States Terminated Historical recordClass II
Pharmatech LLC
- Product
- Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80
- Published
- January 31, 2018
- Distribution
- MI
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Michigan | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
