Ghirardelli Frappe Mix Recall Due to Salmonella Risk
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Ghirardelli Chocolate Company is voluntarily recalling its Perfectly Premium Frappe Mix Chocolate Flavored due to potential Salmonella contamination.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 11, 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 read it as a data point about the issuing system: how quickly FDA detected the hazard, how precise the geographic or product-identifier scope is, and whether similar notices have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action, a single localized FDA recall is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.
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What Happened
Ghirardelli Chocolate Company initiated a voluntary recall of its chocolate flavored frappe mix due to potential contamination with Salmonella. The recall is classified as Class I.
Which Products Are Affected
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.42kg with UPC 747599662003. Affected lots and Best if Used By dates: S397261 (2/28/2027), S397262 (4/30/2027), S397263 (6/30/2027). A total of 309 cases (1,854 units) were distributed.
Distribution includes AK, AZ, CA, FL, GA, ID, IL, IN, KY, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI in the U.S., and Canada, Guatemala, Japan, Philippines, United Kingdom, South Korea.
What You Should Do
Consumers should not consume the affected product.
Why This Matters
Class I recalls involve products that may cause serious adverse health consequences or death.
Source
FDA recall number H-0842-2026 (event ID 98851).
Original source: FDA Official Notice ↗
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