[pending] Product Name: Allura Xper FD10C; Model number: 722001;
Pending LLM rewrite. Source: FDA_DEVICE Z-1062-2026.
- Product
- Product Name: Allura Xper FD10C; Model number: 722001;
- Category
- Medical Device
- 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.
Minimum severity
Pending LLM rewrite. Source: FDA_DEVICE Z-1062-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1079-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1064-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1089-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1057-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1040-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1069-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1051-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1024-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1077-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1049-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1065-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1070-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1100-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1086-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1084-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1020-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1093-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1018-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1076-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1058-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1045-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1091-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1048-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1041-2026.