The Recall Desk

Hazard

Sildenafil recalls

76 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
76
Critical
33
Severe
43
Most recent
2026-10-14

Of the 76 sildenafil recalls we have scored against our rubric, 33 (43%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 43 (57%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all sildenafil 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.

76–76 of 76

  • SevereFDA (Drugs)·D-1699-2012·2012-10-03

    Man King Capsules Recalled for Unapproved Sildenafil Presence

    The FDA is recalling Man King Capsules because they contain sildenafil, an unapproved active ingredient. Consumers should stop using the product.

    Product
    Man King Capsules, 2800 mg, boxes of 5 packets, OTC, Developed by: American Wanbao Pharmaceutical International Group and Hainan Wanbao Biological Engineering Co., Ltd., 27 Heping Road, Haikou, Henan Province, UPC 9 009900 0032328
    Category
    Drug
    Distribution
    Distributed nationwide