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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91451

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

Open FDA event record

Event summary

Timeline bucket
January 13, 2023
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Nephron Sc 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

Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator (racephedrine, USP 11.25), 30x0.5 mL Sterile Vials each in a foil pouch, NDC 0487-2784-01 UPC 3 04872 78401 4

D-0175-2023
Recall number
D-0175-2023
Initiated
January 13, 2023
Classification
Class II
Status
Terminated
Recalling firm
Nephron Sc Inc
Quantity
387,000 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Short Fill

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Short Fill

Code information

Lot #: 126451 Exp. 04/30/2023

Distribution pattern

Nationwide within the United States including Puerto Rico. Guatamala

drug · product 2 of 2

S2 Racepinephrine Inhalation Solution, USP 2.25% Bronchodilator 30x0.5 mL Sterile Unit-of-Use Vials each in a foil pouch, Manufactured By: Nephron West Columbia, SC 29172, NDC 0487-5901-99 UPC 3 04875 90199 9

D-0176-2023
Recall number
D-0176-2023
Initiated
January 13, 2023
Classification
Class II
Status
Terminated
Recalling firm
Nephron Sc Inc
Quantity
925,920 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Short Fill

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Short Fill

Code information

Lot #: 126461, 126431 Exp. 04/30/2023

Distribution pattern

Nationwide within the United States including Puerto Rico. Guatamala