Complete Packaging Acidophilus Blend Recall: Undeclared Milk Allergen Risk
Complete Packaging recalls Acidophilus Blend supplements due to undeclared milk allergen. Affected products sold between Dec 2015 and July 2016. Consumers should check labels for Product No. E-420.
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What happened, in plain English
Complete Packaging is recalling Acidophilus Blend supplements because they contain undeclared milk, which can cause allergic reactions in sensitive individuals. This recall affects specific batches sold between December 2015 and July 2016. Read more at govinfonow.com/recall/23395-complete-packaging-acidophilus-blend-recall-undeclared-milk-allergen-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/23395-complete-packaging-acidophilus-blend-recall-undeclared-milk-allergen-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-0049-2017
Cite this page
“Complete Packaging Acidophilus Blend Recall: Undeclared Milk Allergen Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23395-complete-packaging-acidophilus-blend-recall-undeclared-milk-allergen-risk. Based on FDA recall #F-0049-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0049-2017%22&limit=1).
Why it’s dangerous
The supplement contains milk without being declared as an allergen. This can cause allergic reactions in people who are sensitive to milk, including symptoms like hives, swelling, or breathing difficulties.
Who’s affected
People who own or use the recalled Acidophilus Blend supplements (Product No. E-420) are most at risk if they have milk allergies. The recall covers specific batches sold between December 2015 and July 2016.
How to tell if you have this one
Check for the product name 'Acidophilus Blend', 90 capsules, Product No. E-420, in a 225cc HDPE white bottle. The recall covers specific batches sold from December 2015 through July 2016.
- Brand
Complete Packaging- Category
Food
What to do — step by step
Check Product Label
Look for Product No. E-420 on the bottle label to confirm if your supplement is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “nationwide. No foreign or govt/military/VA consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Which batches are affected?
Batches sold from December 2015 through July 2016 with Lot Numbers 24553-295, 24631-328, 24674-344, and 24774-360.
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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-0049-2017 (August 26, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0049-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.