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.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
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 →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- SevereBetter Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- LowMindray ePM Series Patient Monitor Manuals Recalled for Alarm Clarification
FDA (Devices) · 2026-10-14
Similar recalls
- HighMeijer Joint Health Supplement Recalled for Missing Shellfish Allergen Labeling
FDA (Food) · 2020-02-12
- ModerateCardinal Health Recalls Vitamin D3 Tablets Due to Temperature Excursions
FDA (Drugs) · 2021-06-02
- ModerateHealthmaxx Recalls MAX Glucosamine Tablets Due to Mislabeling
FDA (Food) · 2013-10-02
- ModerateBasic Reset Recalls Trim Up Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateSolgar Glucosamine Chondroitin Recalled Due to Wrong Product Packaging Error
FDA (Food) · 2024-02-07
- ModerateHealthmaxx Recalls MAX Brand Glucosamine Tablets Due to Mislabeling
FDA (Food) · 2013-10-02