[pending] Loard's Lime Sherbert - 32 oz
Pending LLM rewrite. Source: FDA_FOOD H-0737-2026.
- Product
- Loard's Lime Sherbert - 32 oz
- Category
- Food
- Distribution
- 0 states
Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Pending LLM rewrite. Source: FDA_FOOD H-0737-2026.
Medline Industries is recalling three models of medical trays due to calibration issues with sterilization equipment that may affect sterility assurance. The recall affects LVAD Driveline Trays and Central Line Dressing Change Trays distributed nationwide.
Pending LLM rewrite. Source: FDA_FOOD H-0687-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0688-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0715-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0756-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0703-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0765-2026.
Medline Industries is recalling eight models of Convenience Kits due to calibration issues with sterilization equipment that may have affected the sterility assurance level of the devices.
Pending LLM rewrite. Source: FDA_FOOD H-0730-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0696-2026.
Boston Scientific's LUX-Dx II Plus implantable cardiac monitors may fail to collect PVC Burden data or monitor for abnormal heart rhythms in some upgraded devices, creating potential gaps in patient monitoring.
Pending LLM rewrite. Source: FDA_FOOD H-0707-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0751-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0759-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0752-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0724-2026.
Medline Industries is recalling multiple Convenience Kits nationwide because sterilization equipment calibration issues may have compromised the sterility assurance level of the products, despite exposure to validated sterilization cycles.
Pending LLM rewrite. Source: FDA_FOOD H-0689-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0758-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0733-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0753-2026.
Pending LLM rewrite. Source: NHTSA 25V876000.
Pending LLM rewrite. Source: NHTSA 25V872000.
Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.