Exact FDA event identifier

Event 68089

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

Event summary

Timeline bucket: May 12, 2014
Product types: Drug
Classifications: Class I
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

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

0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015

D-1550-2014

Recall number: D-1550-2014
Initiated: May 12, 2014
Classification: Class I
Status: Terminated
Recalling firm: Baxter Healthcare Corp.
Quantity: 4,200 containers

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; blue polyisoprene shavings found inside the bag port tubes

Code information

Lot C931923, exp 8/31/2015

Distribution pattern

Nationwide