FDAClass IIAugust 5, 2020

Progesterone Modified Release 200 mg Capsule recall

Progesterone Modified Release 200 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

Why was Progesterone Modified Release 200 mg Capsule recalled?

Lack of Processing Controls (lack of assurance of conformity to specifications).

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

02-05-2020:30@19, BUD 8/3/2020

Product
Progesterone Modified Release 200 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
Recalling firm
MasterPharm LLC
Quantity
900 capsules
Distribution
Nationwide in the U.S.
Recall date
August 5, 2020
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls