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.
Siemens is recalling Dimension Vista HbA1c reagent cartridges because whole blood samples from Small Sample Containers may produce inaccurate HbA1c values.
Trumpf Medical Systems is recalling 184 TITAN Operating Room Tables due to unintended movement during surgery caused by damaged remotes.
Martin Avenue Pharmacy is voluntarily recalling Atropine sulfate 2 mg/mL injectable vials due to quality control issues that risk sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including triamcinolone injection solutions, due to quality control issues affecting sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling compounded morphine sulfate injectables due to quality control observations that present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including chlorhexidine gluconate ophthalmic solution, due to quality control issues affecting sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling benzalkonium chloride water for injection due to quality control issues affecting sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling compounded Testosterone cypionate 200 mg/mL injections due to quality control observations that present a risk to sterility assurance.
Ikea North America is recalling organic elk-shaped pasta sold in 21 states due to undeclared soy, a major food allergen.
Martin Avenue Pharmacy is voluntarily recalling Pilocarpine 0.25% ophthalmic solution due to quality control issues that risk sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Atropine sulfate 0.5% ophthalmic solution due to quality control issues affecting sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling dexamethasone sodium phosphate injectable vials due to quality control issues that risk sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling trimethoprim/sulfadiazine excipient stock solution injections due to quality control issues that risk sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including Quad mix 1, due to quality control observations that present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Lidocaine 1% injectable vials due to quality control observations that present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling bacteriostatic water for injection due to quality control issues affecting sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Tri-mix T108 injectable vials due to quality control observations that present a risk to sterility assurance.
Jayco is recalling 2015 Jay Flight trailers because cargo capacity labels may overstate load limits, creating a risk of tire failure and crashes.
Jayco is recalling 268 model year 2015 Eagle fifth wheel trailers because incorrect weight calculations on the cargo label could lead to overloading and tire failure.
Navistar is recalling certain IC buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.
Navistar is recalling specific IC school buses because wheelchair lift platform side plates may crack. This defect could cause the platform to fall, increasing the risk of injury to the operator.
Thor Motor Coach is recalling 215 model year 2015 motorhomes because awning mounting brackets may crack, causing the awning to fall and potentially injure people.
Triumph is recalling 417 model year 2014-2015 motorcycles because the engine control unit may improperly activate fuel injectors, potentially causing unexpected power loss.
Eldorado is recalling 2014-2015 Krystal K40 vehicles because a fuel filter defect may cause the engine to stall unexpectedly, increasing crash risk.
Visonic is recalling Amber Pendants and Kits because battery drain may shorten the low-battery warning period. No injuries have been reported.