TRADER JOES A Dozen Sweet Bites Chocolate and Coffee Opera Cake, Raspberry ...
FDA Recall #F-2143-2015 — Class II — April 15, 2015
Recall Summary
| Recall Number | F-2143-2015 |
| Date Initiated | April 15, 2015 |
| Classification | Class II |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | PROLAINAT |
| Location | Aubiet, N/A |
| Country | France |
Product Description
TRADER JOES A Dozen Sweet Bites Chocolate and Coffee Opera Cake, Raspberry Macaroon Cake, Caramel & Chocolate Cake, 9.16 oz UPC 00967679 or SKU 096767.
Reason for Recall
Prolainat is recalling all lots of 9.16 oz packages of Trader Joes A Dozen Sweet Bites (Chocolate & Coffee Op¿ra Cake, Raspberry Macaron Aux Framboises Cake, Caramel & Chocolate Cake) due to undeclared coconut.
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
US
Product Quantity
22,968 units
Product Codes / Lot Numbers
Batch No. 01613PR 01713PR 01813PR 04413PR 04513PR 04613PR 04913PR 04613PR 04931PR 07313PR 07413PR 07713PR 07813PR 11613PR 11913PR 12713PR 11913PR 12013PR 12213PR 11613PR 13413PR 18613PR 18213PR 18313PR 18413PR 22613PR 22413PR 22513PR 22613PR 22813PR 13612 PR 32012PR 01513PR 01613PR 01613PR 01713PR 03713PR 04413PR 04513PR 07413PR 07713PR 07813PR 12213PR 17913PR 18213PR 18313PR 18413PR 17913PR 18313PR 18413PR 22513PR 23413PR 26113PR 22513PR 22613PR 23113PR 23213PR 23313PR 25913PR 25913PR 26013PR 26213PR 01014PR 01214PR 01414PR 03414PR 03514PR 03014PR 03114PR 05114PR 05714PR 09414PR 05214PR 05114PR 05714PR 09714PR 09714PR 09814PR 09914PR 13614PR 13914PR 14014PR 14114PR 14214PR 14314PR 13914PR 16814PR 16914PR 17014PR 02914PR 17014PR 17114PR 17614PR 19214PR 23014PR 24414PR 24414PR 24514PR 24614PR 26213PR 01014PR 01314PR 01014PR 03414PR 03514PR 03614PR 05014PR 05114PR 05614PR 05714PR 09814PR 14014PR 13614PR 09414PR 13914PR 16814PR 16914PR 17014PR 17114PR 17414PR 02914PR 09414PR 19014PR 19114PR 24514PR 24614PR 14214PR 14314PR 18814PR 18914PR 19114PR 01215PR 01315PR 01415PR 02015PR 03015PR 03315PR 03615PR 19114PR 24614PR 01315PR 01215PR 02015PR 03015PR 03315PR
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.