A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Infants’ TYLENOL Oral Suspension, 1 oz. Grape: Recall – Dosing System Complaints. According to the Food & Drug Administration FDA’s MedWatch:
Reports of dosing syringe flow restrictor being pushed into the bottle when inserting the syringe.
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Infants’ TYLENOL Oral Suspension, 1 oz. Grape: Recall – Dosing System Complaints.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
If you have thoughts on the drug or medical device recall or safety alert, share your drug or medical device recall or safety alert comments below.