Mineralife LLC Recall: The dietary supplement product is potentially contaminated with Pseudomonas aeruginosa - F-1305-2019
United States
TerminatedClass II
- Company
- Mineralife LLC
- Product
- Trace Minerals Dietary Supplement , 16.2 fl oz (480 mL) bott…
- Recall date
- October 15, 2018
- Terminated
- April 6, 2021
- Source
- FDA
Reason for recall
The dietary supplement product is potentially contaminated with Pseudomonas aeruginosa
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Trace Minerals Dietary Supplement , 16.2 fl oz (480 mL) bottles, Packaged in dark blue plastic bottles, For freshness, keep refrigerated after opening | Not published in this source record | 515 boxes | Lots: 0818-01 and 0218-01 |
Distribution
- Nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1305-2019
- Event ID
- 82460
- Status
- Terminated
- Classification
- Class II
- Company
- Mineralife LLC
- Product description
- Trace Minerals Dietary Supplement , 16.2 fl oz (480 mL) bottles, Packaged in dark blue plastic bottles, For freshness, keep refrigerated after opening
- Quantity
- 515 boxes
- Reason
- The dietary supplement product is potentially contaminated with Pseudomonas aeruginosa
- Recall initiation date
- October 15, 2018
- Report date
- May 1, 2019
- Classification date
- Not published in this source record
- Termination date
- April 6, 2021
- Distribution pattern
- Nationwide.
- UPC, lot, and code information
- Lots: 0818-01 and 0218-01
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Mineralife LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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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?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of April 6, 2021.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.