Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96209

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

Open FDA event record

Event summary

Timeline bucket
February 07, 2025
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Aspen Biopharma Labs Pvt., Ltd.

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

6 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 6

Bimatoprost NDC# 82187-1001-1 Container description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping.

D-0260-2025
Recall number
D-0260-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
400.0 gm

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot Numbers: HABTC0020123, exp. date Dec-2026 HABTC0050623, exp. date May-2027 HABTC0091023, exp. date Sep-2028

Distribution pattern

Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

drug · product 2 of 6

Alprostadil Container Description: Amber color bottle

D-0261-2025
Recall number
D-0261-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
3.0 gm

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot Numbers: HAALC0020922 exp. date AUG-2025

Distribution pattern

Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

drug · product 3 of 6

Finasteride NDC# 82187-1003-1 Container Description: The product packed in white poly bag containing black poly bag and tied each individual finally packed in HDPE container for shipping.

D-0262-2025
Recall number
D-0262-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
120.0 kg

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot Numbers: HAFSC0040923, exp. date Aug-2027 HAFSC0050923, exp. date Aug-2027

Distribution pattern

Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

drug · product 4 of 6

Chlorambucil Container Description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping.

D-0263-2025
Recall number
D-0263-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
5.1 kg

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot Numbers: HACUC0010722, exp. date Jun-2025 HACUC0010123, exp. date Dec-2025

Distribution pattern

Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

drug · product 5 of 6

Latanoprost NDC# 82187-1002-1 Container Description: Amber colour bottle

D-0264-2025
Recall number
D-0264-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
150.0 gm

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot Numbers: HALAC0010123, exp. date Dec-2026 HALAC0050923, exp. date Aug-2027

Distribution pattern

Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

drug · product 6 of 6

Voriconazole Container Description: voriconazole The product packed in white poly bag containing black poly bag and tied each individual finally packed in HDPE container for shipping.

D-0265-2025
Recall number
D-0265-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
4.0 kg

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations

Code information

Lot Number: HAVZC0020922, exp. date AUG-2026

Distribution pattern

Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

Field note

Send feedback

We'll only use this to respond to your feedback.