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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82538

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

Open FDA event record

Event summary

Timeline bucket
March 25, 2019
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Lohxa LLC

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

Bismuth Subsalicylate Oral Suspension 262mg/15mL, unit dose cups, OTC, Rpkg. By.: Lohxa Worcester, MA, NDC 70166-059-01

D-1130-2019
Recall number
D-1130-2019
Initiated
March 25, 2019
Classification
Class II
Status
Terminated
Recalling firm
Lohxa LLC
Quantity
5 boxes - 250 unit dose cups.

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Labeling: Incorrect or Missing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.

Code information

Lot#: M030042P, Exp. 01/2020

Distribution pattern

MA, NY and WY

drug · product 2 of 2

Phenobarbital Oral Solution, USP 20 mg/5mL, unit dose cup, Rx Only, Rpkg. By.Lohxa Worcester, MA 01608 NDC 70166-536-02

D-1131-2019
Recall number
D-1131-2019
Initiated
March 25, 2019
Classification
Class II
Status
Terminated
Recalling firm
Lohxa LLC
Quantity
46 boxes - 1380 unit dose cups

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Labeling: Incorrect or Missing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.

Code information

Lot# M12031, Exp. 12/2019; T01241 Exp. 02/2020

Distribution pattern

MA, NY and WY