Exact FDA event identifier

Event 98689

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

Event summary

Timeline bucket: March 31, 2026
Product types: Drug
Classifications: Class III
Statuses: Ongoing
Recalling firm wording: Avantor Performance Materials LLC

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

Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC 10106-2448-1

D-0488-2026

Recall number: D-0488-2026
Initiated: March 31, 2026
Classification: Class III
Status: Ongoing
Recalling firm: Avantor Performance Materials LLC
Quantity: 36 bottles

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

Subpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Subpotent drug

Code information

Lot 23G3161005, Exp 9/21/2027

Distribution pattern

Nationwide in the USA, Belgium and France