Home › Recall events › Progressive Laboratories, Inc recall — Thyroid Resilience…
Progressive Laboratories, Inc recall — Thyroid Resilience 120 count bottle packaged in an amber plastic…
FDA (enforcement) · March 21, 2018 · Class I
- Progressive Laboratories, Inc recalled Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap — an FDA enforcement event posted , classified Class I, covering 4 product entries.
- FDA-stated reason: Recalled dietary supplements may contain undeclared milk.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- Progressive Laboratories, Inc
- Source ID
- 79350
FDA Enforcement Report search →
Product entries (4)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-0912-2018 | Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap | Lot # 2072237 | Nationwide through the United States |
| F-0913-2018 | Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap | Lot # 2114667 and 2061167 | Nationwide through the United States |
| F-0914-2018 | Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap | Lot # 2071887 | Nationwide through the United States |
| F-0915-2018 | Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap | Lot # 2071957 and 2082387 | Nationwide through the United States |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
Related: Undeclared-allergen recalls · Food recalls · All recall events