FDA recall record

RB Manufacturing Schiff Move Free Advanced Plus MSM & Vitamin D3 with recall — FDA F-2250-2017

RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.

Class IIIclassification
F-2250-2017official record ID
May 31, 2017report date

Recall record at a glance

Official recordF-2250-2017
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmRB Manufacturing LLC
Report dateMay 31, 2017
Recall initiation dateMay 8, 2017
Quantity288 cases
LocationSalt Lake City, UT, United States

Official product description

Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873

Why the product was recalled

RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.

Distribution information

Nationwide. States included are CA, TX, MO, HI, NV, WA, AZ, CO. No foreign or VA/govt/military consignees.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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