Pennsylvania recalls
3,594 federal recalls affecting Pennsylvania in the last 12 months - 382 Pennsylvania-specific plus 3,212 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 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-FoodJoy GourmetClass IIJoy Saffron Cardamom Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Orange Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Peach Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods Mint Lassi recalled for pasteurization issue
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods Masala Chaash Lassi recalled for pasteurization risk
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy GourmetClass IIJoy Plain Chaash Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Mango-Pina-Orange Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Mango-Pina-Strawberry Lassi recalled for pasteurization risk
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Strawberry Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Pineapple Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods salty lassi recalled for pasteurization risk
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Gourmet Foods Sweet Lassi recalled for pasteurization risk
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Rose Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 2026-07-01FDA-FoodJoy Gourmet FoodsClass IIJoy Mango Lassi recalled for inadequate pasteurization
Product not adequately pasteurized
- 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
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