Fresh Recalls

FDAClass II · Food · Recall H-1174-2026 · Recalled July 22, 2026

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT recall — AMY'S KITCHEN INC.

Agency report date: July 22, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT
Company / brand
AMY'S KITCHEN
Lot / serial / date codes
LOT: 60D0924 BEST BEFORE: 4/2027
Distribution
Domestic: AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, MD, ME, MI, MO, NC, NH, NJ, NV, NY, OH, PA, SC, SD, TN, TX, VA, WA, WI. Foreign: Canada.
Agency product description and boundaries

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes. Let sit 1 minute. Stir. Serve. Stovetop: Heat soup in a saucepan, stirring occasionally. AMY'S KITCHEN, INC. P.O. BOX 7129 PETALUMA, CA 94955 UPC (for U.S. product): 042272005833 UPC (for Canada product): 10042272905833

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Potential for spoilage.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT

3. Open the official notice or contact

Official recall ID
H-1174-2026
Brand
AMY'S KITCHEN
Classification
Class II
Units affected
15,350 cases (12 cans/case)
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Petaluma, CA, United States
Firm address
109 Kentucky St, 94952-2303

Identifying details (verbatim from the notice)

Product codes / lots
LOT: 60D0924 BEST BEFORE: 4/2027
Distribution
Domestic: AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, MD, ME, MI, MO, NC, NH, NJ, NV, NY, OH, PA, SC, SD, TN, TX, VA, WA, WI. Foreign: Canada.
Firm notified the public via
E-Mail
FDA event ID
99306
Recall initiated
June 22, 2026
FDA classified
July 14, 2026
FDA report date
July 22, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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