The Recall Desk
ModerateFDA (Drugs)·D-1434-2020·Announced 2020-08-05

MasterPharm Recalls Progesterone Capsules Due to Processing Control Deficiencies

MasterPharm LLC is recalling Progesterone Modified Release 200 mg Capsules because the company lacks processing controls to ensure the product meets specifications.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or specific contamination, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

MasterPharm LLC is voluntarily recalling Progesterone Modified Release 200 mg Capsules, 90 capsules per bottle. The recall was initiated because the firm identified a lack of processing controls, which means there is no assurance that the product conforms to its required specifications.

The affected product is distributed nationwide in the United States. The specific lot code is 02-05-2020:30@19, with a best-use date of 8/3/2020. The total quantity involved in the recall is 900 capsules.

Consumers who have this product should stop using it and contact MasterPharm LLC at (866) 630-5600 for instructions on how to return the product or obtain a refund.

The recalled product

Product
Progesterone Modified Release 200 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
Manufacturer
MasterPharm LLC
Category
Drug — Prescription Medication
Hazard
Affected units
900

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • 02-05-2020:30@19
  • BUD 8/3/2020

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 26 recalled by MasterPharm LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 26 products in this recall →

Related recalls

Same manufacturer · MasterPharm LLC

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Same hazard · lack of processing controls

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