💊 Tylenol Extra Strength Recalled for Defective Packaging
Some bottles may not fully close, risking accidental exposure.
Johnson & Johnson’s McNeil Consumer Healthcare Division has voluntarily recalled a limited number of Tylenol Extra Strength caplets (500mg, 24-count bottles) because of a defective container. The cap may not secure properly, potentially exposing children or pets to the medication.
The recall affects 3,186 bottles. The recall is nationwide in scope, but so far, distribution of the affected lot (EJA022) has only been confirmed in Colorado, Illinois, Ohio, and Indiana. No injuries or adverse events have been reported. The recall is precautionary.
👉 TABLE OF CONTENTS
📰 WHAT’S HAPPENING
🔍 HOW TO IDENTIFY
🚫 WHAT TO DO
🧽 HOW TO CLEAN
☎️ WHO TO CONTACT
📊 COMPANY HISTORY
💊 THE BIGGER PICTURE
🧾 NOTES AND DISCLAIMER
✅ QUICK HELP CHECKLIST
🔗 SOURCES (OFFICIAL)
