Exact FDA event identifier

Event 68669

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

Event summary

Timeline bucket: June 25, 2014
Product types: Drug
Classifications: Class I
Statuses: Terminated
Recalling firm wording: Pharmacy Creations

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

Ascorbic Acid 500 mg/mL Sterile Injection, 50 mL Multi-dose Vial, Rx only, Pharmacy Creations, Randolph, NJ 07869.

D-1546-2014

Recall number: D-1546-2014
Initiated: June 25, 2014
Classification: Class I
Status: Terminated
Recalling firm: Pharmacy Creations
Quantity: 70 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

mold contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility: Pharmacy Creations is recalling Ascorbic Acid 500 mg/mL 50 mL vials due to mold contamination.

Code information

Lot: 06062014@8, Do Not Use Beyond 12/03/2014

Distribution pattern

NY, NJ, and Puerto Rico