What happened
Original notice title
DaVinci Laboratories Issues Allergy Alert on Undeclared Shellfish Allergen in Amyloid Complete Product Lot 549853001
From the archived source record
When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. More Recalls, Market Withdrawals, & Safety Alerts Recalls, Market Withdrawals, & Safety Alerts Recall Resources Enforcement Reports Industry Guidance For Recalls Major Product Recalls DaVinci Laboratories, a division of FoodScience, LLC of Williston, Vermont is recalling 72 bottles of Amyloid Complete because it may contain undeclared shellfish (Shrimp and Crab). People who have an allergy or severe sensitivity to shellfish run the risk of serious or life-threatening allergic reaction if they consume these products. The issue was identified through a customer complaint which found bottles of Amyloid Complete may contain Perna Plus Tabs with DMG, resulting in undeclared shellfish. No illnesses have been reported to date. Follow FDA Follow @US_FDA on X Follow FDA on Facebook Follow @FDArecalls on X Recent Recalled Product Photos on FDA's Flickr Photostream Recent Recalled Product Photos on FDA's Flickr Photostream
What the official notice says to do
Check the original notice for the instructions that apply to the named product, company, and affected lots.
Read the official notice →Status and source details
- Status recorded in the archive
- Published recall notice
- Source checked
- Jul 16, 2026
- Record revision
- 0235b8faa2e2
This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.
Sources, dates, and coverage →