Wawa Fruit Punch Pint Recall for Undeclared Milk Allergen
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Wawa Beverage Company is recalling 1,694 units of Wawa Fruit Punch Pint (16oz) due to undeclared milk allergen. The Class I recall affects products distributed in DE, MD, NJ, PA, and VA.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 23, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
Wawa Beverage Company initiated a voluntary recall of Wawa Fruit Punch Pint (16oz) plastic bottles because the product contains an undeclared milk allergen.
Which Products Are Affected
- Product: Wawa Fruit Punch Pint (16oz), Plastic bottle
- UPC: 726191018432
- Quantity: 1,694 units
- Distribution: DE, MD, NJ, PA, VA
- Recall Number: H-0858-2026
What You Should Do
Consumers should not consume the product. Check purchased items against the UPC and discard or return affected products.
Why This Matters
This is a Class I recall involving a potential serious health risk from undeclared allergens.
Source
FDA recall H-0858-2026 (report date 20260603)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (685 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to June 23, 2026.
Frequently Asked Questions
Common questions about this FDA recall.