Schiff Move Free Advanced Plus Tablets Recall: Incorrect Packaging
Schiff is recalling 80-tablet dietary supplements due to incorrect packaging. Consumers should check product labels for lot number AAM600 to determine if affected.
Lower-risk recall
RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
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What happened, in plain English
Schiff is recalling a dietary supplement product because of incorrect packaging. This issue does not pose a safety risk but may affect product labeling and consumer confidence. Read more at govinfonow.com/recall/21374-schiff-move-free-advanced-plus-tablets-recall-incorrect-packaging.
Source Summary by GovInfoNow · govinfonow.com/recall/21374-schiff-move-free-advanced-plus-tablets-recall-incorrect-packaging · Updated October 8, 2026 · FDA enforcement record: FDA #F-2250-2017
Cite this page
“Schiff Move Free Advanced Plus Tablets Recall: Incorrect Packaging.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21374-schiff-move-free-advanced-plus-tablets-recall-incorrect-packaging. Based on FDA recall #F-2250-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2250-2017%22&limit=1).
Why it’s dangerous
The product has incorrect packaging, which means the labeling may not accurately reflect the contents. This could lead to confusion about the product's ingredients or dosage, but it does not cause physical harm.
Who’s affected
People who purchased Schiff Move Free Advanced Plus MSM & Vitamin D3 with Gluc:osamine + Chondroitin supplements containing lot number AAM600 are affected. Those most at risk are consumers who rely on the product for dietary needs.
How to tell if you have this one
Check the product label for the lot number AAM600. The product is a dietary supplement with 80 coated tablets, sold under the Schiff brand.
- Brand
Schiff- Category
Food
What to do — step by step
Check Product Label
Look for the lot number AAM600 on the packaging to confirm if the product is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 8 states.
FDA distribution: “Nationwide. States included are CA, TX, MO, HI, NV, WA, AZ, CO. No foreign or VA/govt/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Colorado, Hawaii, Missouri, Nevada, Texas, Washington.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- 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-2250-2017 (May 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2250-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.