Exact FDA event identifier

Event 98795

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

Event summary

Timeline bucket: April 28, 2026
Product types: Drug
Classifications: Class I
Statuses: Ongoing
Recalling firm wording: B BRAUN MEDICAL INC

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

Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.

D-0540-2026

Recall number: D-0540-2026
Initiated: April 28, 2026
Classification: Class I
Status: Ongoing
Recalling firm: B BRAUN MEDICAL INC
Quantity: 95,412 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.

Code information

Lot #:J4P756, J4S843, Exp 5/31/2027

Distribution pattern

U.S.A. Nationwide