Island Pacific Imitation Crab Flakes Recall
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Shandong Ling Xian Food Co.,LTD is recalling 751 cartons of Island Pacific Imitation Crab Flakes distributed in California due to undeclared sodium tripolyphosphate.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 11, 2026 and geographically references California. Its severity classification of "low" 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
The recall was initiated due to undeclared sodium tripolyphosphate (STTP) in the product.
Which Products Are Affected
Island Pacific IMITATION CRAB FLAKES NET WT: 1.0 LB (454g), UPC: 0000000175012. Code info: Crab Flake 2603062605JS. Expiration dates: 17/06/2026, 25/06/2026, 08/10/2027, 05/03/2028. Quantity: 751 cartons. Distributed domestically in CA. Product of China. Recall number H-1184-2026. Recalling firm: Shandong Ling Xian Food Co.,LTD, Rizhao, China.
What You Should Do
No specific consumer action steps are provided in the recall notice.
Why This Matters
The recall affects products distributed in California and involves a labeling issue with a food additive.
Source
FDA recall H-1184-2026 (Class III), report date 20260729.
Original source: FDA Official Notice ↗
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