Exact FDA event identifier

Event 91520

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

Event summary

Timeline bucket: January 13, 2023
Product types: Drug
Classifications: Class III
Statuses: Terminated
Recalling firm wording: OurPharma 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

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

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

FentaNYL Citrate 2.5mg/50mL (50mcg/mL) Injection Solution, Preservative-Free IV Injection 50mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1001-01.

D-0172-2023

Recall number: D-0172-2023
Initiated: January 13, 2023
Classification: Class III
Status: Terminated
Recalling firm: OurPharma LLC
Quantity: 768 cassettes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Short Fill: Underfilled units.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Short Fill: Underfilled units.

Code information

Lots: 100122080003, Exp. 2/26/2023; 100122090001, Exp. 3/07/2023; 100122100002, Exp. 4/05/2023

Distribution pattern

IL and MO