FDA recall record

Synergy Rx RETINOIC ACID SOLUTION in all strengths including 0.3%, 0.4%, 0.5%, 1%, RETINOIC recall — FDA D-0542-2017

Lack of Assurance of Sterility: There are also CGMP Deviations.

Class IIclassification
D-0542-2017official record ID
Mar 22, 2017report date

Recall record at a glance

Official recordD-0542-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSynergy Rx
Report dateMar 22, 2017
Recall initiation dateFeb 10, 2017
QuantityN/A
LocationSan Diego, CA, United States

Official product description

RETINOIC ACID SOLUTION in all strengths including 0.3%, 0.4%, 0.5%, 1%, RETINOIC ACID SOLUTION LIQUID, 0.4%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

Why the product was recalled

Lack of Assurance of Sterility: There are also CGMP Deviations.

Distribution information

Nationwide within the United States

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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