Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.

Class I - Dangerous
💊 Drugs Recalled: January 18, 2013 Aaron Industries Other Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot# 71648, 68088; FP-47-041-02535
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Aaron Industries Inc
Reason for Recall:
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.

Product Codes/Lot Numbers:

Lot# 71648, 68088; FP-47-041-02535

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-187-2013

Related Recalls

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.

Apr 11, 2014 Over-the-Counter Nationwide View Details →

Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is precipitating out.

Feb 4, 2014 Over-the-Counter Nationwide View Details →

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.

Apr 4, 2013 Over-the-Counter Nationwide View Details →