RECALL RECORD — CLASS IIRecall closedF-2953-2017/FDA enforcement

Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point Brand

What you need to know

Class II
  • What happened

    Undeclared milk. Goose Point Steamers in 5 Clams in Butter & Garlic Sauce is recalled because label declared butter, cream, or dairy but milk is NOT declared.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAIN, AZ, CA, ID +3 moreMore food

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Product identification

Source: FDA FOOD

Brand nameNisbet Oyster Co INC
Recalling firmNisbet Oyster Co INCBay Center, WA, United States
UPC / barcodes
0 92206 16101 2
Lot / date codes
  • Lot codes: AJT28AUG2017 AJT32AUG 2017 AJT33SEP2017 AJU34SEP2017 AKV53SEP2017 ALV53SEP2017 CMV70SEP2017 DMV71OCT2017 DMV71SEP2017 DMW74OCT2017 DNW83OCT2017 DOW75OCT2017 DOW89OCT2017 EOQOCT2017 EOX102NOV2017 EOX98OCT2017 FRY139DEC2016 FRY139DEC2017 FRY140DEC2017 FRZ 161DEC2018 FRZ140DEC2017 FRZ160DEC2016 FRZ160DEC2017 FRZ161DEC2017 FRZ161DEC2017 FRZ165JAN2018 IWC246MAR2018 JWC250MAR2018 JWC250MAR2018 JXC251APR2018 KXC263APR2018 KYC263APR2019 KYC264APR2018 KYC265APR2018 KYD266JUN2018 LAE362JUL2018 LZD312JUN2018 LZD312JUN2018 MBE16JUL2018 MCF18AUG2018 MCF18JUL2018 MCF30SEP2018 NCF30SEP2018 NCF32SEP2018 NCF33OCT2018 NCF33SEP2018 NCF47OCT2018 NCP30SEP2018 OEG109NOV2018 PFH117NOV2018 XEQ328MAY17 YFR349JUN2017
Distribution area
INAZCAIDORTXWA

distributed in AZ, CA, ID, OR, TX, and WA.

United States

Quantity affected4610 cases (12/1 lb. packages per case)
Recall initiationFDA report date: August 9, 2017
FDA recall numberF-2953-2017

Beyond the headline

The recall, in context

Nisbet Oyster Co INC initiated this food recall on July 3, 2017. The FDA enforcement report states: Undeclared milk. Goose Point Steamers in 5 Clams in Butter & Garlic Sauce is recalled because label declared butter, cream, or dairy but milk is NOT declared. The FDA report lists distribution as: distributed in AZ, CA, ID, OR, TX, and WA.

The FDA enforcement report describes the reason as: Undeclared milk. Goose Point Steamers in 5 Clams in Butter & Garlic Sauce is recalled because label declared butter, cream, or dairy but milk is NOT declared.

Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point Brand was made or distributed by Nisbet Oyster Co INC in Bay Center, WA, United States. This page reflects FDA report F-2953-2017, dated August 9, 2017.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point Brand recall?

Nisbet Oyster Co INC recalled Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point Brand in an FDA Class II enforcement action reported as F-2953-2017. Undeclared milk. Goose Point Steamers in 5 Clams in Butter & Garlic Sauce is recalled because label declared butter, cream, or dairy but milk is NOT declared.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Nisbet Oyster Co INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-2953-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.