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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 88457

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

Open FDA event record

Event summary

Timeline bucket
August 06, 2021
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
XELLIA PHARMACEUTICALS USA, 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

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

Micafungin for Injection, 50 mg/vial, Single-Dose Vial, Sterile, Rx Only, For Intravenous Infusion Only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089. NDC 70594-036-01

D-0756-2021
Recall number
D-0756-2021
Initiated
August 06, 2021
Classification
Class II
Status
Terminated
Quantity
9,161 vials 50 mg and 100 mg vials total

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Labeling; Incorrect or Missing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.

Code information

Lot 467111, exp 1/2023

Distribution pattern

Nationwide USA

drug · product 2 of 2

Micafungin for Injection, 100 mg/vial, Single-Dose Vial, Sterile, Rx Only, For Intravenous Infusion Only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089. NDC 70594-037-01

D-0757-2021
Recall number
D-0757-2021
Initiated
August 06, 2021
Classification
Class II
Status
Terminated
Quantity
9,161 (50mg and 100 mg vials total)

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Labeling; Incorrect or Missing

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.

Code information

Lot 467111, exp 1/2023

Distribution pattern

Nationwide USA