Schiff Move Free Advanced Tablets Recalled for Incorrect Packaging
RB Manufacturing is recalling Schiff Move Free Advanced Plus MSM & Vitamin D3 tablets due to incorrect packaging.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III and is due to incorrect packaging, which is a packaging-only problem with no reported health hazards.
Plain-English summary
RB Manufacturing is recalling Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets. The recall is being conducted because of incorrect packaging.
The affected product is identified by Lot Number AAM600. The recall involves 288 cases of the dietary supplement. Distribution was nationwide, specifically in California, Texas, Missouri, Hawaii, Nevada, Washington, and Colorado. There were no foreign or VA/govt/military consignees.
Consumers with this product should check the packaging and lot number. If the product matches the description, they should stop using it and follow the instructions provided by the recalling firm or the FDA.
The recalled product
- Product
- Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873
- Manufacturer
- RB Manufacturing LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 288
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Number: AAM600
Distribution
Related recalls
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02