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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71749

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

Open FDA event record

Event summary

Timeline bucket
July 17, 2015
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

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

0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B0043, NDC 0338-0553-18.

D-1335-2015
Recall number
D-1335-2015
Initiated
July 17, 2015
Classification
Class I
Status
Terminated
Recalling firm
Baxter Healthcare Corp.
Quantity
133,600 bags

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: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Code information

Lot#: P327635, Exp 12/15

Distribution pattern

Nationwide

drug · product 2 of 2

0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.

D-1336-2015
Recall number
D-1336-2015
Initiated
July 17, 2015
Classification
Class I
Status
Terminated
Recalling firm
Baxter Healthcare Corp.
Quantity
189,120 bags

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: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Code information

Lot#: P319921, Exp 12/15

Distribution pattern

Nationwide