FDA Recall United States Terminated Historical recordClass I
Progressive Laboratories, Inc
- Product
- Xenesta Nuvive Womens 90 count packaged in a white plastic b…
- Published
- March 21, 2018
- Distribution
- Nationwide
Progressive Laboratories, Inc Recall: Recalled dietary supplements may contain undeclared milk.
United States
TerminatedClass I
- Company
- Progressive Laboratories, Inc
- Product
- Thyroid Resilience 120 count bottle packaged in an amber pla…
- Recall date
- February 23, 2018
- Terminated
- August 7, 2018
- Source
- FDA
Reason for recall
Recalled dietary supplements may contain undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap | Not published in this source record | 469 bottles | Lot # 2114667 and 2061167 |
Distribution
- Nationwide through the United States
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0913-2018
- Event ID
- 79350
- Status
- Terminated
- Classification
- Class I
- Company
- Progressive Laboratories, Inc
- Product description
- Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap
- Quantity
- 469 bottles
- Reason
- Recalled dietary supplements may contain undeclared milk.
- Recall initiation date
- February 23, 2018
- Report date
- March 21, 2018
- Classification date
- Not published in this source record
- Termination date
- August 7, 2018
- Distribution pattern
- Nationwide through the United States
- UPC, lot, and code information
- Lot # 2114667 and 2061167
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- 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 79350 with 3 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
Progressive Laboratories, Inc
- Product
- Xenesta Nuvive Mens 90 count packaged in an white plastic bo…
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Progressive Laboratories, Inc
- Product
- Testosterzone 180 count bottle packaged in an amber plastic…
- Published
- March 21, 2018
- Distribution
- Nationwide
Responsible company: Progressive Laboratories, Inc
Other recalls from Progressive Laboratories, Inc
FDA Recall United States Terminated Historical recordClass I
Progressive Laboratories, Inc
- Product
- Xenesta Nuvive Womens 90 count packaged in a white plastic b…
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Progressive Laboratories, Inc
- Product
- Xenesta Nuvive Mens 90 count packaged in an white plastic bo…
- Published
- March 21, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Progressive Laboratories, Inc
- Product
- Testosterzone 180 count bottle packaged in an amber plastic…
- Published
- March 21, 2018
- Distribution
- Nationwide
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
