Exact FDA event identifier

Event 76681

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

Event summary

Timeline bucket: April 02, 2016
Product types: Drug
Classifications: Class I
Statuses: Ongoing
Recalling firm wording: Complete Pharmacy and Medical Solutions 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

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

D-0918-2017

Recall number: D-0918-2017
Initiated: April 02, 2016
Classification: Class I
Status: Ongoing
Recalling firm: Complete Pharmacy and Medical Solutions LLC
Quantity: 49 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.

Code information

Lot # 22016, Exp 1/30/2017

Distribution pattern

Nationwide and Puerto Rico