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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91142

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

Open FDA event record

Event summary

Timeline bucket
November 09, 2022
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Lannett Company 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

Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10

D-0160-2023
Recall number
D-0160-2023
Initiated
November 09, 2022
Classification
Class III
Status
Terminated
Recalling firm
Lannett Company Inc.
Quantity
5,640 bottles

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Impurity/Degradation Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurity/Degradation Specifications

Code information

Lots: 20256318A (12/2022), 20256321A (12/2022), 21000238A (01/2023)

Distribution pattern

Nationwide USA

drug · product 2 of 2

Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10

D-0161-2023
Recall number
D-0161-2023
Initiated
November 09, 2022
Classification
Class III
Status
Terminated
Recalling firm
Lannett Company Inc.
Quantity
20,040 bottles

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Failed Impurity/Degradation Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Impurity/Degradation Specifications

Code information

Lots: 21000279A (exp 01/2023), 20256320A (12/2022)

Distribution pattern

Nationwide USA