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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 72102

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

Open FDA event record

Event summary

Timeline bucket
August 21, 2015
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Nephron Pharmaceuticals Corp.

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, Starter Kit (Racepinephrine 11.25 mg) 10 individual foil wrapped vials with 1 EZ Breathe Atomizer per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-10

D-0388-2016
Recall number
D-0388-2016
Initiated
August 21, 2015
Classification
Class II
Status
Terminated
Quantity
47,754 cartons

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Discoloration

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Discoloration

Code information

Lots R4027A (Exp 10/31/2015), R4036A (Exp 12/31/2015)

Distribution pattern

Nationwide

drug · product 2 of 2

Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Refills (Racepinephrine USP 11.25 mg), 30 individual foil wrapped vials per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-01

D-0389-2016
Recall number
D-0389-2016
Initiated
August 21, 2015
Classification
Class II
Status
Terminated
Quantity
32,490 cartons

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Discoloration

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Discoloration

Code information

Lots R4016A (Exp 08/31/2015), R4017A (Exp 08/31/2015), R4035A (Exp 12/31/2015)

Distribution pattern

Nationwide