Atlanta Ingredients Recalls Frozen Lemon Poppy Seed Muffin Mix for Plastic Hazard
Atlanta Ingredients recalls frozen, unbaked lemon poppy seed muffin mix due to potential plastic contamination. Check your freezer for affected batches.
Stop using this now
Frozen, unbaked muffins potentially contaminated with small pieces of plastic.
Contact the company
What happened, in plain English
Atlanta Ingredients is recalling a specific batch of frozen, unbaked lemon flavored poppy seed muffin mix because it may contain small pieces of plastic. The product was distributed to grocery store distribution centers in several states for use in retail baking departments. Consumers should check their freezers for the affected item. Read more at govinfonow.com/recall/16954-atlanta-ingredients-recalls-frozen-lemon-poppy-seed-muffin-mix-for.
Source Summary by GovInfoNow · govinfonow.com/recall/16954-atlanta-ingredients-recalls-frozen-lemon-poppy-seed-muffin-mix-for · Updated October 11, 2026 · FDA enforcement record: FDA #F-1983-2019
Cite this page
“Atlanta Ingredients Recalls Frozen Lemon Poppy Seed Muffin Mix for Plastic Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/16954-atlanta-ingredients-recalls-frozen-lemon-poppy-seed-muffin-mix-for. Based on FDA recall #F-1983-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1983-2019%22&limit=1).
Why it’s dangerous
The frozen, unbaked muffins may be contaminated with small pieces of plastic. Ingesting these plastic fragments can pose a choking or internal injury hazard to consumers.
Who’s affected
Grocery stores and consumers who purchased or received this specific frozen muffin mix from distribution centers in CA, IA, MA, MN, PA, NJ, and UT. Individuals are at risk of ingesting plastic pieces if the product is prepared and eaten.
How to tell if you have this one
Look for '48534 MDM 10200921, Natural and Artificial Lemon Flavored Poppy Seed Muffin, pre - deposited - unbaked - keep frozen' with UPC 10035074485344. The net weight is 25.3 lbs, manufactured by CSM Bakery Products NA, Inc. in Tucker, GA. Check for Batch# 1000690578 and a Best By Date of 12/29/2019.
- Brand
Atlanta Ingredients- Product
48534 MDM 10200921, Natural and Artificial Lemon Flavored Poppy Seed Muffin, pre - deposited - unbaked - keep frozen- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Distributed to grocery store distribution centers in CA, IA, MA, MN, PA, NJ, and UT for baking in baking departments of retail grocery stores.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1982-2019 | 48533 MDM 10200917, Double Dutch Muffin, pre - deposited - unbaked - keep frozen, UPC 10035074485337, Net Wt. 25.3 lbs, Manufactured by CSM Bakery Products NA, Inc. Tucker, GA; Batch# 1000686280, Best By Date 12/29/2019 | 320 cases |
| F-1983-2019 | 48534 MDM 10200921, Natural and Artificial Lemon Flavored Poppy Seed Muffin, pre - deposited - unbaked - keep frozen, UPC 10035074485344, Net Wt. 25.3 lbs, Manufactured by CSM Bakery Products NA, Inc. Tucker, GA; Batch# 1000690578, Best By Date 12/29/2019 | 402 cases |
What to do — step by step
Stop Using the Product
Do not prepare or consume the recalled frozen muffin mix due to the risk of plastic contamination.
Discard or Return Item
The recall record does not specify a return or disposal method, but the product should be kept away from consumption.
Where it went and when
Where it was distributed
Distributed in 7 states.
FDA distribution: “Distributed to grocery store distribution centers in CA, IA, MA, MN, PA, NJ, and UT for baking in baking departments of retail grocery stores.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Iowa, Massachusetts, Minnesota, New Jersey, Pennsylvania, Utah.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-1983-2019 (July 12, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1983-2019 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.