Clean & Clear advantage, 3-in-1 foaming wash 8 FL. OZ. (240 mL) bottle, OTC, Distributed in the ...

FDA Drug Recall #D-098-2013 - Class III, December 4, 2012

Recall Summary

Recall Number D-098-2013
Classification Class III, Low risk
Date Initiated December 4, 2012
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Johnson & Johnson
Location Skillman, NJ
Product Type Drugs
Quantity 1,474,462 bottles

Product Description

Clean & Clear advantage, 3-in-1 foaming wash 8 FL. OZ. (240 mL) bottle, OTC, Distributed in the US by: Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies Inc. Skillman, NJ 08558-9418 NDC 58232-0326-8

Reason for Recall

Superpotent (Single Ingredient Drug): salicylic acid

Distribution Pattern

Nationwide

Lot / Code Information

0142VA, 0132VB, 0112VC, 0122VB, 0102VA, 0102VB, 0112VB 0122VA, 0092VB, 0112VA, 0092VA, 0082VA, 0072VA, 0062VA 0062VB, 0052VA, 0052VB, 0042VA, 0032VA, 0022VA, 0012VA, 0171VA, 0171VB, 0161VB, 0151VA, 0161VA, 0141VA, 0131VA 0131VB, 0121VA, 0111VA, 0101VA, 0091VA, 0081VB, 0081VA 0071VA, 0061VA, 0051VB, 0051VA, 0041VA, 0031VA, 0021VB 0011VC, 0011VB, 0190VA, 0011VA, 0180VB, 0170VB, 0180VA 0722RT, 0732RT, 0742RT, 0752RT, 1722RD, 1732RD, 1772RD 1782RD, 1792RD, 1802RD, 1802RDA, 1812RD, 1822RD, 0092RD, 0102RD, 0112RD, 0122RD, 0132RD, 0142RD, 0162RD 0172RD, 0182RD, 0192RD, 0212RD, 0202RD, 0062RD, 1451RD 1461RD, 1461RDA, 1511RD, 1521RD, 1531RD, 1661RD, 1481RD, 1571RD, 1581RD, 1591RD, 1601RD, 1611RD, 1621RD 1681RD, 1532RD, 1522RD, 1842RD, 1512RD, 1522RD, 1562RD 1582RD, 1572RD, 1722RD, 1732RD, 1742RD, 1772RD, 1782RD 1792RD, 1802RD, 1812RD, 1812RDA, 1822RD, 1842RD, 1852RD, 1872RD

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Frequently Asked Questions

Stop taking the medication and contact your pharmacist or doctor immediately. For Class I recalls, this is urgent. For Class II or III recalls, consult your doctor before stopping, abruptly discontinuing certain medications (blood pressure drugs, antidepressants, diabetes medications) can be more harmful than continuing while arranging a replacement. Check whether the recall applies to your specific lot number and expiration date. Return the product to your pharmacy and report any adverse effects to FDA MedWatch at 1-800-FDA-1088.

Not necessarily. Many drug recalls are initiated because of quality system failures or test results that suggest a product might not meet specifications, even if no patients have reported harm. The FDA uses a precautionary approach: if there is reason to believe quality standards were not met, a recall is required regardless of whether adverse effects have been reported. Class I recalls typically involve a reasonable probability of harm; Class II recalls may cause temporary health issues; Class III recalls are for products unlikely to cause adverse health consequences but that still violate regulations.

Pharmacies typically receive recall notices directly from drug wholesalers and manufacturers within days of the recall being announced. Your pharmacist can look up whether any product in your prescription history matches a recalled lot number. For current recalls, the FDA publishes updates at FDA.gov/safety/recalls-market-withdrawals-safety-alerts and sends MedWatch email alerts for significant drug safety issues. You can sign up for MedWatch alerts at FDA.gov. Most major pharmacy chains also have their own recall notification systems that automatically alert pharmacists when a recalled product is in their inventory.

What Should You Do?

Stop using this medication if affected by this recall. Contact your pharmacist or prescribing doctor immediately for guidance. Do not flush medications, use a drug take-back program.