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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98856

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

Open FDA event record

Event summary

Timeline bucket
April 27, 2026
Product types
Drug
Classifications
Class III
Statuses
Ongoing
Recalling firm wording
Golden State Medical Supply 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

Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05

D-0534-2026
Recall number
D-0534-2026
Initiated
April 27, 2026
Classification
Class III
Status
Ongoing
Quantity
8,526 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Code information

Lot#: GS066750, GS067084, GS067710, GS067873, Exp 3/31/2028; GS068339, GS068897, Exp 8/31/2028

Distribution pattern

USA Nationwide

drug · product 2 of 2

Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01

D-0535-2026
Recall number
D-0535-2026
Initiated
April 27, 2026
Classification
Class III
Status
Ongoing
Quantity
1,620 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Code information

Lot #: GS067909, Exp 4/30/2028; GS068646, Exp 8/31/2026

Distribution pattern

USA Nationwide