Illinois recalls
4987 federal recalls on file affecting Illinois - 1002 Illinois-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars recalled for Salmonella risk
Potential Salmonella contamination
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).
Potential Salmonella contamination
- 2026-07-01FDA-FoodChampion FoodsClass IINationwideMotor City Pizza Co. 5 Cheese Bread recalled for Salmonella risk
potential salmonella contamination
- 2026-07-01FDA-FoodPrime Food ProcessingClass IPrime Food Processing dried herring recalled for botulism risk
Improperly eviscerated which may result in Clostridium botulinum contamination
- 2026-07-01FDA-DrugSun PharmaceuticalClass IINationwideSun Pharmaceutical Perampanel recalled for tablet strength mix-up
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.
- 2026-07-01FDA-DrugElevate Oral CareClass IINationwideElevate Oral Care Povi-One recalled for sub-potency
sub potency
- 2026-07-01FDA-DrugAnnora PharmaClass IINationwideCamber Lacosamide tablets recalled for Selexipag mix-up
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep FREPP Clear recalled for sterility concerns
Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep Clear recalled for fungal contamination risk
Non-Sterility: Due to presence of Aspergillus penicillioides.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep FREPP Clear recalled for sterility risk
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for sterility assurance concern
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
- 2026-07-01FDA-DrugANI PharmaceuticalsClass IIINationwideANI Pharmaceuticals hydroxyzine solution recalled for foreign substance
Presence of foreign substance
- 2026-07-01FDA-DrugDirect RxClass IINationwideDirect Rx Duloxetine D/R recalled for impurity risk
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar cinacalcet tablets recalled for manufacturing deviations
CGMP Deviations
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Corlanor recalled for foreign substance contamination
Presence of Foreign Substance.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar tablets recalled for manufacturing deviations
CGMP Deviations
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar recalled for manufacturing quality deviations
CGMP Deviations
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Corlanor heart medication recalled for foreign substance
Presence of Foreign Substance.
- 2026-07-01FDA-DrugAjanta PharmaClass IINationwideAjanta Pharma fenofibrate capsules recalled for quality issues
CGMP Deviations
- 2026-07-01FDA-DrugThe Harvard DrugClass IINationwideMajor Pharmaceuticals Methylergonovine Maleate recalled for subpotency
Subpotent Drug
- 2026-06-25FDA-PRRevival Animal HealthNationwideBreeder's Edge and Shelter's Choice dog milk replacers recalled for vitamin D risk
Revival Animal Health of Orange City, IA is recalling Breeder’s Edge® Foster Care® Canine, Shelter’s Choice® Canine Milk Replacers, and is expanding the current recall to include the Breeder’s Edge® Foster Care® GM (goat milk) products due to variable levels of Vitamin D resulting in either low or e
- 2026-06-25FDA-PRLehi Valley TradingNationwideHigh Valley Orchard raisins recalled for undeclared peanuts
June 25, 2026, Lehi Valley Trading Company of Mesa, AZ, is recalling 624 units of its 15 ounce packages of High Valley Orchard Chocolate Covered Raisins because they contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they
- 2026-06-25USDAPrivate SelectionPublic Health AlertPrivate Selection chicken breast recalled for undeclared eggs
Misbranding Unreported Allergens
- 2026-06-25CPSCTreatlifeNationwideTreatlife smoke and CO detectors recalled for fire alert failure
The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns.
- 2026-06-25CPSCDaikinNationwideAmana air conditioners and heat pumps recalled for fire risk
The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers.
- 2026-06-25CPSCABGA Advanced TradingNationwideHonlyne LED party favors recalled for battery ingestion risk
The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-06-25CPSCSmall FishNationwideSmall Fish Busy Board recalled for magnet ingestion risk
The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
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