PlainRecalls
FDA Drug Critical Class I Terminated

All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or green background, the product is included in the recall.

Reported: May 2, 2018 Initiated: March 15, 2018 #D-0697-2018

Product Description

All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or green background, the product is included in the recall.

Reason for Recall

Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages, with a green or orange Bayer logo located on the lower left corner of the front of the carton, because the ingredients on the front sticker may not match the actual product in the carton.

Details

Units Affected
188,631 units
Distribution
Nationwide in the USA
Location
Whippany, NJ

Frequently Asked Questions

What product was recalled?
All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or green background, the product is included in the recall.. Recalled by Bayer HealthCare Pharmaceuticals, Inc.. Units affected: 188,631 units.
Why was this product recalled?
Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages, with a green or orange Bayer logo located on the lower left corner of the front of the carton, because the ingredients on the front sticker may not match the actual product in the carton.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 2, 2018. Severity: Critical. Recall number: D-0697-2018.