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Lower risk Food recall · FDA · Published September 19, 2019

A Priori Specialty Foods recalls razor clams with unknown object in tin

A Priori Specialty Foods recalls Espinaler Razor Clams (Trimmed) 4/6 Classic Line due to an unknown object found in some tins. Consumers should check for N4R-LE7R on tin or E7R MM/YYYY on box.

🇺🇸 FDA recall #F-0012-2020FoodA Priori Specialty Foods ›
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Recalling firmYTM, Inc. DBA A Priori Specialty Foods314 W 300 S Bsmt · Salt Lake City, UT 84101-1943
✎ GovInfoNow plain-language explainer

What happened, in plain English

A Priori Specialty Foods is recalling Espinaler Razor Clams (Trimmed) 4/6 Classic Line because an unknown object was found in some tins. This could pose a risk of choking or injury if the object is sharp or small enough to be swallowed. Read more at govinfonow.com/recall/16637-a-priori-specialty-foods-recalls-razor-clams-with-unknown-object.

Source Summary by GovInfoNow · govinfonow.com/recall/16637-a-priori-specialty-foods-recalls-razor-clams-with-unknown-object · Updated October 5, 2026 · FDA enforcement record: FDA #F-0012-2020

Cite this page

“A Priori Specialty Foods recalls razor clams with unknown object in tin.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16637-a-priori-specialty-foods-recalls-razor-clams-with-unknown-object. Based on FDA recall #F-0012-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0012-2020%22&limit=1).

Why it’s dangerous

The recall is due to an unknown object being found in some tins. This object could be small enough to be swallowed, potentially causing choking or injury. The hazard is not specified as causing serious injury in normal use.

Who’s affected

Anyone who purchased the Espinaler Razor Clams (Trimmed) 4/6 Classic Line from the manufacturer. Children and individuals with small hands are at higher risk of choking if the unknown object is swallowed.

How to tell if you have this one

Check for the code N4R-LE7R printed on the tin or E7R MM/YYYY printed on the box. The product is sold in 120g aluminum tins in paper cartons.

  • Brand
    A Priori Specialty Foods
  • Product
    Espinaler Razor Clams (Trimmed) 4/6 Classic Line, " N4R-LE7R printed on the tin AND/OR E7R MM/YYYY printed on the box
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check for Recalled Product

    Look for the code N4R-LE7R on the tin or E7R MM/YYYY on the box.

Where it went and when

Where it was distributed

Distributed in 11 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “North America  AZ, CA, HA, IA, MA, NC, NY, PA, SC, UT, VA, WA and Ontario, Canada. No govt/VA/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Iowa, Massachusetts, New York, North Carolina, Pennsylvania, South Carolina, Utah, Virginia, Washington.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Sep 19, 201912. FDA classified it Class II: Oct 3, 201923. Published in FDA’s Enforcement Report: Oct 9, 201934. FDA terminated the recall: May 28, 2020420192020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0012-2020 (September 19, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0012-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA