[pending] Grizzly Industrial Recalls Heavy-Duty Planers Due to Impact and Laceration Hazards
Pending LLM rewrite. Source: CPSC 26134.
- Product
- G0815 15" 3HP Heavy-Duty Planers
- Category
- Consumer Product
- Distribution
- Distributed nationwide
Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Pending LLM rewrite. Source: CPSC 26134.
Pending LLM rewrite. Source: CPSC 26128.
Pending LLM rewrite. Source: CPSC 26132.
Pending LLM rewrite. Source: CPSC 26133.
Pending LLM rewrite. Source: CPSC 26127.
Pending LLM rewrite. Source: CPSC 26129.
Pending LLM rewrite. Source: FDA_DEVICE Z-0673-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0589-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0691-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0595-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0618-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0600-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0196-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0626-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0624-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0702-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0587-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0647-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0659-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0648-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0667-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0712-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0179-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0599-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0724-2026.