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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98596

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 17, 2026
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Nephron SC, 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

1 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 1

Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172, NDC 69374-330-05.

D-0479-2026
Recall number
D-0479-2026
Initiated
March 17, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Nephron SC, LLC
Quantity
146,280 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Labelling: Illegible label

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labelling: Illegible label

Code information

Lot AB6001, exp date 1/15/2027

Distribution pattern

Nationwide within the United States