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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79350

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 23, 2018
Product types
Food
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Progressive Laboratories, Inc

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 4

Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap

F-0912-2018
Recall number
F-0912-2018
Initiated
February 23, 2018
Classification
Class I
Status
Terminated
Quantity
669 bottles

App-derived interpretation

Undeclared allergen reason.undeclared_allergen · v1.0.0
undeclared milk

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled dietary supplements may contain undeclared milk.

Code information

Lot # 2072237

Distribution pattern

Nationwide through the United States

food · product 2 of 4

Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap

F-0913-2018
Recall number
F-0913-2018
Initiated
February 23, 2018
Classification
Class I
Status
Terminated
Quantity
469 bottles

App-derived interpretation

Undeclared allergen reason.undeclared_allergen · v1.0.0
undeclared milk

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled dietary supplements may contain undeclared milk.

Code information

Lot # 2114667 and 2061167

Distribution pattern

Nationwide through the United States

food · product 3 of 4

Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap

F-0914-2018
Recall number
F-0914-2018
Initiated
February 23, 2018
Classification
Class I
Status
Terminated
Quantity
88 boxes (2 bottles/box)

App-derived interpretation

Undeclared allergen reason.undeclared_allergen · v1.0.0
undeclared milk

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled dietary supplements may contain undeclared milk.

Code information

Lot # 2071887

Distribution pattern

Nationwide through the United States

food · product 4 of 4

Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap

F-0915-2018
Recall number
F-0915-2018
Initiated
February 23, 2018
Classification
Class I
Status
Terminated
Quantity
147 boxes (2 bottles/box)

App-derived interpretation

Undeclared allergen reason.undeclared_allergen · v1.0.0
undeclared milk

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Recalled dietary supplements may contain undeclared milk.

Code information

Lot # 2071957 and 2082387

Distribution pattern

Nationwide through the United States