Guzzler Kiwi-Strawberry (American Beverage) – Nozzle Cap Hazard (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Guzzler Kiwi-Strawberry, 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
Brand
American Beverage Corp
Lot Codes / Batch Numbers
018397000022
Products Sold
The following product bearing a "best buy" or "expiration date" earlier than 09/24/12 ONLY: Flavor and UPC code: Kiwi-Strawberry, 018397000022
American Beverage Corp is recalling Guzzler Kiwi-Strawberry, 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporat due to There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing) then possibly ingested,. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a possibility that a part of the nozzle cap of the bottle can become dislodged through abuse (i.e. excessive chewing) then possibly ingested, and posing a potential health/safety hazard. The cap in question is no longer used by ABC and was last produced in September of 2011. Firm does not anticipate finding any impacted product in the market.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026