Product Recall Detail
Product Recall Detail
Alka Seltzer Plus Day & Night Cold Formula Liquid Gels 20 ct (recalled Dec. 9, 2009)
| PRODUCT |
SIZE |
LOT NUMBER |
UPC |
| Alka Seltzer Plus Day & Night Cold Formula Liqui-Gels | 20 ct. | 296939L | 0-16500-53777-9 |
Reason for Recall:
Bayer HealthCare is voluntarily recalling the produt because it is mislabelled. The company reports that in a limited number of combination packages of Alka-Seltzer Plus Day and Night Cold Formula Liquid Gels from a single lot, the information on the underside of the blister package was reversed. Therefore, the label for the green Night product appears under some of the blue Day product and vice versa. As such, there is a risk that consumers may not be aware of the warnings of an antihistamine in the product that could cause drowsiness.
What to do:
Consumers should stop using the product and contact Bayer's Consumer Relations Call Center at (800) 986-3307 Monday - Friday 8:30am - 5:30pm. Any consumer with a medical concern or questions should contact their healthcare provider.
Contact information:
Contact Bayer's Consumer Relations Call Center at (800) 986-3307 Monday - Friday 8:30am - 5:30pm.
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