Premier Research Labs LLC Recall: Product spoiling over time; spoilage visible beneath lid/closure upon opening.
United States
TerminatedClass II
- Company
- Premier Research Labs LLC
- Product
- AloePro Dietary Supplement Made With Organic ALOE VERA LIQUI…
- Recall date
- June 15, 2022
- Terminated
- April 30, 2024
- Source
- FDA
Reason for recall
Product spoiling over time; spoilage visible beneath lid/closure upon opening.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| AloePro Dietary Supplement Made With Organic ALOE VERA LIQUID 16 FL Oz. (475 mL) PREMIER RESEARCH LABS UPC Code: 80773500137 packaged in plastic HDPW bottles | Not published in this source record | 6,784 units | Lot 122121-0137 FCE#20921, Item Number 0137, |
Distribution
- Nationwide throughout the US
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1418-2022
- Event ID
- 90491
- Status
- Terminated
- Classification
- Class II
- Company
- Premier Research Labs LLC
- Product description
- AloePro Dietary Supplement Made With Organic ALOE VERA LIQUID 16 FL Oz. (475 mL) PREMIER RESEARCH LABS UPC Code: 80773500137 packaged in plastic HDPW bottles
- Quantity
- 6,784 units
- Reason
- Product spoiling over time; spoilage visible beneath lid/closure upon opening.
- Recall initiation date
- June 15, 2022
- Report date
- July 20, 2022
- Classification date
- Not published in this source record
- Termination date
- April 30, 2024
- Distribution pattern
- Nationwide throughout the US
- UPC, lot, and code information
- Lot 122121-0137 FCE#20921, Item Number 0137,
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Premier Research Labs LLC
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.
