The Recall Desk
ModerateFDA (Drugs)·D-1437-2020·Announced 2020-08-05

MasterPharm Recalls Tadalafil 18 mg Capsules Due to Processing Control Deficiencies

MasterPharm LLC is recalling Tadalafil 18 mg capsules nationwide due to a lack of processing controls that ensures conformity to 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, but the source text does not report any illnesses, injuries, or hospitalizations. The hazard is a theoretical risk related to processing controls rather than a confirmed high-risk pathogen or structural defect, fitting the criteria for a moderate severity score.

Plain-English summary

MasterPharm LLC is voluntarily recalling Tadalafil 18 mg capsules, 90 capsules per bottle, distributed nationwide in the United States. The recall is being conducted due to a lack of processing controls, which means there is a lack of assurance that the product conforms to its specifications.

The affected product is identified by the following lot codes and expiration dates: 01-23-2020:33@15 (BUD 7/21/2020), 02-07-2020:48@3 (BUD 8/5/2020), and 02-26-2020:09@15 (BUD 8/24/2020). The total quantity involved in this recall is 900 capsules.

Consumers who have purchased this product should stop using it and contact MasterPharm LLC at (866) 630-5600 for further instructions or a refund. The company is located at 115-02 Liberty Ave, Richmond Hill, NY 11419.

The recalled product

Product
Tadalafil 18 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 (4)

  • 01-23-2020:33@15
  • BUD 7/21/2020 02-07-2020:48@3
  • BUD 8/5/2020 02-26-2020:09@15
  • BUD 8/24/2020

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 →

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