Food, drugs, devices › Pharm D Solutions, LLC
Drug recall: Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop
FDA enforcement event 75552 is a drug recall by Pharm D Solutions, LLC of Houston, TX, initiated 12 Oct 2016 and classified Class III, with 2 product records.
FDA defines Class III as a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences. 43% of the 288 drug enforcement events initiated in 2016 carry the same class.
Status: Terminated, terminated 11 May 2017. Initiation: voluntary: firm initiated. Pharm D Solutions, LLC has 4 enforcement events on this register, with a median of 18 product records per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Pharm D Solutions, LLC, Houston, TX.
Reason for recall
"Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct"
Distribution
"AZ and WA"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| D-0426-2017 | 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 | 4 mL: 510 vials, 5 mL: 486 vials | Class III | Terminated | 18 Jan 2017 |
| D-0427-2017 | 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 | 112 bottles | Class III | Terminated | 18 Jan 2017 |
Context
Other enforcement events for Pharm D Solutions, LLC
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 23 May 2019 | Bacteriostatic Water for Injection, 10 mL vials, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6 | Drug | Class II | 18 |
| 19 Nov 2018 | Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 | Drug | Class II | 1 |
| 10 Sep 2018 | Acetylcysteine Injection 10 mg/5 mL (2 mg/mL), Pharm D Solutions, Houston, Texas ---- NDC 69699-1424-10 | Drug | Class II | 79 |
All 4 events for Pharm D Solutions, LLC
Questions and answers
Why was this drug recalled?
FDA's record gives the reason for recall as: "Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct"
What does Class III mean?
FDA classifies recalls by relative degree of health hazard. Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
Where was the product distributed?
FDA's distribution pattern field reads: "AZ and WA"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 11 May 2017. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA drug enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.