Bomunity Ltd Co Recall: Potential to be contaminated with bacteria
United States
TerminatedClass II
- Company
- Bomunity Ltd Co
- Product
- Paximune Dietary Supplement Contains Bovine Proteins that he…
- Recall date
- June 4, 2021
- Terminated
- September 23, 2021
- Source
- FDA
Reason for recall
Potential to be contaminated with bacteria
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz. (60ml) packaged in dark glass bottle 12 bottles per case UPC 64395 00001 | Not published in this source record | 3540 cases | LOT 210402 |
Distribution
- Nationwide throughout the US
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0817-2021
- Event ID
- 88151
- Status
- Terminated
- Classification
- Class II
- Company
- Bomunity Ltd Co
- Product description
- Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz. (60ml) packaged in dark glass bottle 12 bottles per case UPC 64395 00001
- Quantity
- 3540 cases
- Reason
- Potential to be contaminated with bacteria
- Recall initiation date
- June 4, 2021
- Report date
- August 11, 2021
- Classification date
- Not published in this source record
- Termination date
- September 23, 2021
- Distribution pattern
- Nationwide throughout the US
- UPC, lot, and code information
- LOT 210402
- 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: Bomunity Ltd Co
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.
