Island Pacific Imitation Crab Sticks Recall
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Shandong Ling Xian Food Co.,LTD is recalling 751 cartons of Island Pacific Imitation Crab Sticks 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
Shandong Ling Xian Food Co.,LTD initiated a voluntary recall of Island Pacific Imitation Crab Sticks because the product contains undeclared sodium tripolyphosphate (STTP).
Which Products Are Affected
The recall involves Island Pacific IMITATION CRAB STICKS NET WT: 1.0 LB (454g) with UPC: 0000000175029. Affected product is from Crab Stick Lot No.: 2412292402HS. A total of 751 cartons were distributed to California.
What You Should Do
Consumers should not consume the product. Contact information for returns or refunds is not provided in the recall notice.
Why This Matters
The undeclared ingredient poses a potential risk for individuals with sensitivities to sodium tripolyphosphate.
Source
FDA recall number H-1182-2026
Original source: FDA Official Notice ↗
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