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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82918

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

Open FDA event record

Event summary

Timeline bucket
May 21, 2019
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Heritage Pharmaceuticals, 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

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

PROCHLORPERAZINE EDISYLATE INJECTION, USP 10 mg/2mL (5mg/mL), 2mL Vial, Rx Only, Mfg by: Emcure Pharmaceuticals Ltd., Hinjawadi, Pune, India. Mfg for: Heritage Pharmaceuticals Inc. NDC 23155-294-31

D-1397-2019
Recall number
D-1397-2019
Initiated
May 21, 2019
Classification
Class I
Status
Terminated
Quantity
55,480 2 mL vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial growth

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate Injection, USP 1gm/4 mL (250mg/mL) and Prochlorperazine Edisylate Injection, USP 10mg/2mL (5mg/mL) .

Code information

Lot: VPCA172, EXP April 2020

Distribution pattern

Nationwide in the USA

drug · product 2 of 2

AMIKACIN SULFATE INJECTION, USP, 1 gram/4 mL (250 mg/ml), 4 mL vial, Rx only, Mfd. by: Emcure Pharmaceuticals, Ltd., Hinjawadi, Pune, India Mfd. for: Heritage Pharmaceuticals Inc.. NDC 23155-290-32

D-1398-2019
Recall number
D-1398-2019
Initiated
May 21, 2019
Classification
Class I
Status
Terminated
Quantity
14,960 4 mL vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial growth

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate Injection, USP 1gm/4 mL (250mg/mL) and Prochlorperazine Edisylate Injection, USP 10mg/2mL (5mg/mL) .

Code information

Lot: VEAC025, EXP 10-2019

Distribution pattern

Nationwide in the USA

Field note

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