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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73560

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

Open FDA event record

Event summary

Timeline bucket
January 20, 2015
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Pacifico National, Inc. dba AmEx Pharmacy

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

Avastin (Bevacizumab) 2 mg/0.08 mL syringe, Office Administration Only, AmEx Pharmacy, 1515 Elizabeth St Suite J, Melbourne, FL 32901.

D-0869-2016
Recall number
D-0869-2016
Initiated
January 20, 2015
Classification
Class I
Status
Terminated
Quantity
45 syringes

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
bacterial contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility: Product tested positive for bacterial contamination.

Code information

Lot #: 141224C, Exp. 03/24/2015; 150915B, Exp. 12/14/2015

Distribution pattern

Nationwide

drug · product 2 of 2

Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe, Office Administration Only, AmEx Pharmacy, 1515 Elizabeth St Suite J, Melbourne, FL 32901.

D-0870-2016
Recall number
D-0870-2016
Initiated
January 20, 2015
Classification
Class I
Status
Terminated
Quantity
836 syringes

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
bacterial contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility: Product tested positive for bacterial contamination.

Code information

Lot #: 150116B, Exp. 04/16/2015; 150119R, Exp. 04/19/2015; 150316H, Exp. 06/14/2015

Distribution pattern

Nationwide