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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 75552

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

Open FDA event record

Event summary

Timeline bucket
October 12, 2016
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Pharm D Solutions, 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

Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1709-04

D-0426-2017
Recall number
D-0426-2017
Initiated
October 12, 2016
Classification
Class III
Status
Terminated
Recalling firm
Pharm D Solutions, LLC
Quantity
4 mL: 510 vials, 5 mL: 486 vials

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrect/Undeclared Excipient; product description section of testosterone cypionate incorrectly states "in grapeseed oil" instead of "in sesame oil" . The primary panel is correct

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipient; product description section of testosterone cypionate incorrectly states "in grapeseed oil" instead of "in sesame oil" . The primary panel is correct

Code information

Lot: 09122016:34, exp 09/07/2017

Distribution pattern

AZ and WA

drug · product 2 of 2

HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1723-20

D-0427-2017
Recall number
D-0427-2017
Initiated
October 12, 2016
Classification
Class III
Status
Terminated
Recalling firm
Pharm D Solutions, LLC
Quantity
112 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
Labeling; Error

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct

Code information

Lots: 07272016:03 Expiration Date: 01/23/2017 and 09142016:88 Expiration Date: 03/07/2017

Distribution pattern

AZ and WA