[pending] Loard's Strawberry Ice Cream - 32 oz; 56 oz
Pending LLM rewrite. Source: FDA_FOOD H-0752-2026.
- Product
- Loard's Strawberry Ice Cream - 32 oz; 56 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-0752-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0740-2026.
Intuitive Surgical is recalling certain Universal Surgical Manipulator arm sub-assemblies in da Vinci X and Xi Surgical Systems due to screws that may be susceptible to breaking during use.
Pending LLM rewrite. Source: FDA_FOOD H-0734-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0704-2026.
BioFire Diagnostics, LLC is recalling the Spotfire Respiratory/Sore Throat Panel due to false negative test results and control failures that may not accurately detect infections.
Pending LLM rewrite. Source: FDA_FOOD H-0751-2026.
Medline Industries is recalling multiple Convenience Kit medical devices due to calibration issues in sterilization and packaging equipment that may affect sterility assurance. The devices were distributed nationwide.
Pending LLM rewrite. Source: FDA_FOOD H-0695-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0728-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0750-2026.
Medline Industries is recalling Convenience Kits (Model DYKMBNDL200A) due to calibration issues in sterilization equipment that may have compromised sterility assurance. The kits were distributed nationwide.
Erbe Medical is recalling ERBEFLO CleverCap hybrid tubing and cap sets for endoscopes due to a connector configuration that may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
Medline Industries is recalling Triple Lumen Insertion Kits (Model DYNDM1031A) due to calibration issues with sterilization equipment that may have compromised the sterility assurance level of the products.
Pending LLM rewrite. Source: FDA_FOOD H-0689-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0724-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0746-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0687-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0767-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0690-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0757-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0739-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0708-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0738-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0714-2026.