Class II · Moderate risk
Nandrolone Decanoate 200mg/mL
Lack of Assurance of Sterility
Nandrolone Decanoate 200 mg/mL Injectable
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Sterility Assurance.
Cause type: Sterility / contamination
A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.
What was recalled
Nandrolone Decanoate 200 mg/mL Injectable, 10 mL vials, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
Drug: Nandrolone
- Recalling firm
- Pharm D Solutions, LLC
- Origin
- TX, United States
- Initiated by
- FDA Mandated
- FDA recall number
- D-1329-2019 · FDA notice
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Other Nandrolone recalls
See all
Class III · Low risk
Nandrolone Decanoate
Subpotent Drug
Class III · Low risk
Nandrolone Decanoate
Subpotent Drug
Class III · Low risk
Nandrolone Decanoate
Subpotent Drug
Class III · Low risk
Nandrolone Decanoate
Subpotent Drug
Other recalls by Pharm D Solutions, LLC
All 2019 recalls
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Testosterone Cypionate 200 mg/mL
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Testosterone Cyp/Pro 95/5%
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Class II · Moderate risk
Testosterone 200 mg/mL
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