Medications & Supplements/Over-the-Counter

L. Perrigo Company: Zephrex-D Pseudoephedrine HCl Nasal Decongestant Recalled for Microbial Risks

Agency Publication Date: December 21, 2017

Summary

L. Perrigo Company is recalling 19,944 cartons of Zephrex-D (pseudoephedrine HCl) 30 mg Maximum Strength Nasal Decongestant due to microbial contamination. This recall affects softgel tablets sold in 24-count paper cartons that were distributed nationwide. Consumers should immediately stop using the medication and check their packaging for the specific lot number affected to prevent potential infection or health complications.

Risk

The product may contain microbial contamination, which can cause infections or other adverse health effects, particularly in individuals with weakened immune systems or underlying health conditions.

What You Should Do

Identify your product by checking the paper carton for Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, 24 softgel tablets.
Check the packaging for Lot # AF4273A with an expiration date of 02/18.
Look for NDC 70085-151-01 printed on the carton to confirm it is the affected product.
If your product matches these details, stop using the medication immediately.
Contact your healthcare provider or pharmacist for guidance regarding this recall.
Return any unused product to the place of purchase for a refund and contact L. Perrigo Company at 1-888-723-3332 for further instructions.
For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls

Your Remedy Options

Full Refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant (24 softgel tablets)

Model:

NDC 70085-151-01

Lot Numbers:

AF4273A (Exp. 02/18)

Date Ranges: 02/18

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 78520

Status: Resolved

Manufacturer: L. Perrigo Company

Sold By: Perrigo

Manufactured In: United States

Units Affected: 19,944 Cartons (24 tablets each)

Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

Identify your product by checking the paper carton for Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, 24 softgel tablets.

Check the packaging for Lot # AF4273A with an expiration date of 02/18.

Look for NDC 70085-151-01 printed on the carton to confirm it is the affected product.

If your product matches these details, stop using the medication immediately.

Contact your healthcare provider or pharmacist for guidance regarding this recall.

Return any unused product to the place of purchase for a refund and contact L. Perrigo Company at 1-888-723-3332 for further instructions.

For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls