Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96428

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

Open FDA event record

Event summary

Timeline bucket
March 07, 2025
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Mylan Institutional, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Drug 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

2 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.

drug · product 1 of 2

Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-445-20.

D-0290-2025
Recall number
D-0290-2025
Initiated
March 07, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Mylan Institutional, Inc.
Quantity
347 Cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Out of specification

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Super-Potent Drug: Out of specification potency results were obtained.

Code information

Lot 3116074, Exp. 09/30/2025

Distribution pattern

Nationwide in the USA

drug · product 2 of 2

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-443-20.

D-0291-2025
Recall number
D-0291-2025
Initiated
March 07, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Mylan Institutional, Inc.
Quantity
1,068 cartons

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Out of specification

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Super-Potent Drug: Out of specification potency results were obtained.

Code information

Lot 3115773, Exp. 03/31/2025

Distribution pattern

Nationwide in the USA