Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point brand. Product is ...
FDA Recall #F-2953-2017 — Class II — July 3, 2017
Recall Summary
| Recall Number | F-2953-2017 |
| Date Initiated | July 3, 2017 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Nisbet Oyster Co Inc |
| Location | Bay Center, WA |
Product Description
Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point brand. Product is packaged in a plastic tray with heat sealed plastic film and packed in fiber pre-printed retail box. Net wt. 1 lb (454 gram). UPC 0 92206 16101 2. The label is read in parts "****100% NATURAL INGREDIENTS: Clams, Butter (Cream, Salt), Garlic, Modified Food Starch, Natural Butter Flavor, Lemon, Parsley, Citric Acid ***ALLERGENS: This product contains clams & dairy-butter and is produced in a plant that processes other shellfish including oysters, shrimp & crab***".
Reason for Recall
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.
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution Pattern
distributed in AZ, CA, ID, OR, TX, and WA.
Product Quantity
4610 cases (12/1 lb. packages per case)
Product Codes / Lot Numbers
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
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.