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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73235

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

Open FDA event record

Event summary

Timeline bucket
February 05, 2016
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Baxter Healthcare 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

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

0.9% Sodium Chloride Irrigation, USP, 500 mL bottle, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product code 2F7123, NDC 0338-0048-03

D-0731-201
Recall number
D-0731-201
Initiated
February 05, 2016
Classification
Class II
Status
Terminated
Recalling firm
Baxter Healthcare Corp.
Quantity
257,364 bottles

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0
PARTICULATE MATTER

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of particulate matter identified as an insect.

Code information

Lot # G120162, Exp 11/18

Distribution pattern

Nationwide and Puerto Rico