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Safety Alerts
September 14, 1999

Diphenhydramine HCL Capsules Recalled by Mutual Pharmaceutical Company

Philadelphia, PA (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Mutual Pharmaceutical Company is recalling Diphenhydramine HCL Capsules because of low capsule fill weight leading to content uniformity failure.

PRODUCT
Diphenhydramine HCL Capsules, 25 mg, 1,000 capsule bottles, Rx, under the URL label. NDC #0677-0063-10.

Recall #D-417-9.  Class III

CODE
LOT #40977.

MANUFACTURER
Mutual Pharmaceutical Company, Philadelphia, Pennsylvania.

RECALLED BY
Manufacturer, by letter on July 26, 1999. Firm-initiated recall ongoing.

DISTRIBUTION
Indiana.

QUANTITY
Firm estimated that 708 bottles remained on market at time of recall initiation.

Safety Alerts compiles comprehensive safety recall information for the United States. SafeMail is a free email service to warn consumers of faulty products and contaminated foods. For complete information regarding current recalls, past recalls and timely product warning notification visit: www.safetyalerts.com.

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.