Hazard
11 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 11 subpotent ingredient recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all subpotent ingredient recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Optiwize is recalling 78 units of OptiWize Collagen Plus, 320 count, after NSF testing showed the manganese level was below the label quantity.
Medline Industries is recalling Suture Removal Trays because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
Sandoz Inc. is recalling specific lots of Fosinopril Sodium and Hydrochlorothiazide tablets because the hydrochlorothiazide content was subpotent at the 9-month time point.
Stayma Consulting Service is recalling Duet DHA Balanced tablets and softgels because the beta carotene (Vitamin A) content is subpotent.
Stayma Consulting Service is recalling Duet DHA 430 vitamin and Omega-3 products because the beta carotene (Vitamin A) content is subpotent.
Stayma Consulting Service is recalling specific lots of Nata Komplete multi-vitamin tablets because they contain subpotent levels of beta carotene (Vitamin A).
Stayma Consulting Service is recalling Duet DHA 430 ec because the beta carotene (Vitamin A) content is subpotent.
Max Huber Research Labs is recalling LA MER SPF 18 Fluid Tint because the active ingredient avobenzone may be subpotent, potentially reducing the product's sun protection.
Max Huber Research Labs is recalling LA MER SPF 18 Fluid Tint because the active ingredient Avobenzone may be subpotent, reducing sunscreen effectiveness.
Hi-Tech Pharmacal Co., Inc. is recalling 10,440 bottles of Bucalsep Oral Solution because the cetylpyridinium chloride ingredient is subpotent.
L. Perrigo is recalling 60,048 blister packs of PE Daytime Cold/Flu LiqGel because the active ingredient Phenylephrine HCl was subpotent at the 12-month time point.