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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Calvin Scott & Company, Inc.: Weight Loss Medications Recalled for Lack of Stability Studies

Agency Publication Date: October 2, 2020
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Summary

Calvin Scott & Company, Inc. is recalling various lots of Diethylpropion and Phentermine weight loss medications that were repackaged into pouches. These drug products were repackaged without supporting stability studies to ensure the medicine remains safe and effective in this new packaging. The recall affects three specific drug types distributed to physician offices in California, Idaho, Illinois, Oklahoma, and Rhode Island.

Risk

Repackaging drugs into pouches without stability testing means the medication may not maintain its potency or chemical integrity over time. This could lead to consumers receiving ineffective treatment or being exposed to degradation products that have not been safety-tested.

What You Should Do

  1. Check your medication packaging to see if you have Diethylpropion (25 mg or 75 mg) or Phentermine (30 mg) capsules/tablets distributed by Calvin Scott & Co. Inc.
  2. For Diethylpropion 25 mg tablets (NDC 00527-1475-01), check for lot numbers CS19311, CS19337 (Exp 12/20), CS20018B, CS20019, CS20037, CS20075, CS20076, CS20112, CS20169 (Exp 8/21), CS19311 (Exp 12/21), CS20199 (Exp 5/22), or CS20243 (Exp 7/22).
  3. For Diethylpropion 75 mg tablets (NDC 00527-1477-01), check for lot numbers CS19192, CS19226, CS19263 (Exp 10/20), CS19300 (Exp 7/21), CS19338 (Exp 8/21), CS20034 (Exp 10/21), CS20077 (Exp 1/22), or CS20165, CS20241 (Exp 4/22).
  4. For Phentermine 30 mg capsules (NDC 00527-0597-10), check for lot numbers CS19309 or CS20098 with expiration date 12/21.
  5. If your medication is affected, contact your healthcare provider or pharmacist for guidance on continuing your treatment and to report any concerns.
  6. Return any unused product to the place of purchase for a refund and contact Calvin Scott & Company, Inc. at their Albuquerque, NM office for further instructions.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Refund for unused product

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Diethylpropion (25 mg tablets)
Model:
NDC 00527-1475-01
Recall #: D-0009-2021
Lot Numbers:
CS19311 (Exp 12/20)
CS19337 (Exp 12/20)
CS20018B (Exp 8/21)
CS20019 (Exp 8/21)
CS20037 (Exp 8/21)
CS20075 (Exp 8/21)
CS20076 (Exp 8/21)
CS20112 (Exp 8/21)
CS20169 (Exp 8/21)
CS20168 (Exp 12/21)
CS20199 (Exp 5/22)
CS20243 (Exp 7/22)
Date Ranges: Exp 12/20, Exp 8/21, Exp 12/21, Exp 5/22, Exp 7/22
Product: Diethylpropion (75 mg tablets)
Model:
NDC 00527-1477-01
Recall #: D-0010-2021
Lot Numbers:
CS19192 (Exp 10/20)
CS19226 (Exp 10/20)
CS19263 (Exp 10/20)
CS19300 (Exp 7/21)
CS19338 (Exp 8/21)
CS20034 (Exp 10/21)
CS20077 (Exp 1/22)
CS20165 (Exp 4/22)
CS20241 (Exp 4/22)
Date Ranges: Exp 10/20, Exp 7/21, Exp 8/21, Exp 10/21, Exp 1/22, Exp 4/22
Product: Phentermine (30 mg capsules)
Model:
NDC 00527-0597-10
Recall #: D-0011-2021
Lot Numbers:
CS19309 (Exp 12/21)
CS20098 (Exp 12/21)
Date Ranges: Exp 12/21

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86442
Status: Resolved
Manufacturer: Calvin Scott & Company, Inc.
Sold By: Physician consignees
Manufactured In: United States
Distributed To: California, Idaho, Illinois, Oklahoma, Rhode Island

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.