Severity
Low
LowClass IIITerminated
FDA Food recall · Reported May 31, 2017
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873
RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
Rb Manufacturing LLC recalled Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated… - a low-severity action.
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated… was recalled by Rb Manufacturing LLC in May 31, 2017. Reason: RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.. Check the official notice for the remedy. Verify recall #F-2250-2017 with the FDA Food before acting.
The recall
Rb Manufacturing LLC issued this low-severity FDA Food recall-RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging..
- Low
- severity level
- Class III
- classification
- May 31, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2250-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2250-2017) was formally reported on May 31, 2017, with the manufacturer initiating the action on May 8, 2017. It is classified under Low severity (Class III), with a current status of Terminated. Rb Manufacturing LLC is listed as the recalling firm, operating out of Salt Lake City, UT. Federal records list the affected scope as 288 cases.
The documented reason for this recall is: RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging. Distribution data in the federal record shows the product reached: Nationwide. States included are CA, TX, MO, HI, NV, WA, AZ, CO. No foreign or VA/govt/military consignees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
288 cases
Related Recalls
6
6 from same agency
Product description
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873
Reason for recall
RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-2250-2017 |
| Date reported | May 31, 2017 |
| Date initiated | May 8, 2017 |
| Recalling firm | Rb Manufacturing LLC |
| Firm location | Salt Lake City, UT |
| Affected scope | 288 cases |
| Distribution | Nationwide. States included are CA, TX, MO, HI, NV, WA, AZ, CO. No foreign or VA/govt/military consignees. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2250-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873. Recalled by Rb Manufacturing LLC. Units affected: 288 cases.
Why was this product recalled? ▼
RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 31, 2017. Severity: Low. Recall number: F-2250-2017.
Where was the recalled product distributed? ▼
Distribution: Nationwide. States included are CA, TX, MO, HI, NV, WA, AZ, CO. No foreign or VA/govt/military consignees..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2250-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported May 31, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.