Here we go with more recalls. As always, follow the links if you want more information or consult with your own nation's food and beverage safety agencies.
********** Chocolate Recalls **********
Dark Chocolate Raspberry Cups Recall
Mechanicsburg, PA — April 2, 2026 Karns Foods is voluntarily recalling its approximate 8-ounce packages of "Mini Dark Chocolate Raspberry Cups" because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled "Mini Dark Chocolate Raspberry Cups" were distributed to Karns Foods locations in Pennsylvania. The product comes in an 8-ounce, clear plastic package marked with a pack date on September 18, 2025. Approximal 26-42 packs were affected.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the peanut-containing product was distributed in packaging that did not reveal the presence of peanuts as an active ingredient. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's packaging processes.
Products with this pack date were pulled immediately from shelves on January 30, 2026. Notification efforts to registered rewards shoppers who purchased the product were made at that time.
Consumers who have purchased packages of Mini Dark Chocolate Raspberry Cups are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 717-766-6477 8 am – 3 pm Monday -Friday EST.
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ARLINGTON, VA – Lidl US is recalling all lots of their Favorina Chocolate Ladybugs - German-Style Nougat 3.52 oz box UPC 20304492 due to undeclared hazelnut allergen. People who have allergies to hazelnuts run the risk of serious or life-threatening allergic reactions if they consume these products.
The products were distributed between 01/28/2026 - 03/11/2026. The product was distributed to all Lidl US store locations in Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia.
No illnesses have been reported to date.
The recall was initiated after it was discovered that the product containing tree nuts was distributed in packaging that did not reveal the presence of hazelnuts.
If customers have purchased this product, they should not consume it, and immediately return it to their nearest Lidl store for a full refund (a receipt is not required for return). Customers who have questions about this voluntary recall should call the Lidl US Customer Care Hotline at (844) 747-5435 8 am-8 pm ET, Monday - Saturday.
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FOR IMMEDIATE RELEASE – Date – Ferndale, Michigan. Nalpac is voluntarily recalling DTF Sexual Chocolate it purchased and resold. The products have been found to contain sildenafil and tadalafil. Nalpac is not the manufacturer of this product.
Sildenafil and tadalafil are the active ingredients in the FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients could interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels for those individuals who use prescriptions drugs which contain nitrates. Nalpac has not received any reports of adverse events related to this recall.
The recalled product is packaged in cases containing 20 retail units. The product can be identified by UPC 757817783069 on the product label. The product was available for purchase in adult retail stores and through shopsexology.com and royalsins.com. Please find the product label below:
Nalpac is not the Manufacturer of these products but is voluntarily recalling the product, notifying its customers by email and is arranging for return of all recalled products. Consumers and retailers that have the recalled product should stop using or selling products and return to the place of purchase or discard immediately.
Consumers with questions regarding this recall can contact Nalpac by telephone at 248-541-1140 or by email at sales@nalpac.com Monday to Friday from 8:00 am to 4:30 pm eastern. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report:
Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
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