Oregon recalls
4476 federal recalls on file affecting Oregon - 491 Oregon-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-01FDA-DeviceTMJ SolutionsClass IINationwideTMJ Solutions bilateral implant recalled for component mismatch
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
- 2026-07-01FDA-DevicePhilipsClass IINationwidePhilips Avalon Fetal Monitor recalled for speaker connector defect
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
- 2026-07-01FDA-DevicePhilipsClass IINationwidePhilips Avalon FM20 Fetal Monitor recalled for speaker connector defect
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
- 2026-07-01FDA-DeviceIntuitive SurgicalClass IINationwideIntuitive Surgical Da Vinci recalled for E-brake failure risk
Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restricted column range of motion and/or uncontrolled motion, which may cause patient tissue injury/crushing injury/bleeding.
- 2026-07-01FDA-DeviceMedlineClass INationwideMedline Convenience Kits recalled for anesthetic quality issues
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- 2026-07-01FDA-DeviceMedlineClass INationwideMedline Convenience Kits recalled for anesthetic quality issues
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- 2026-07-01FDA-DeviceMedlineClass INationwideMedline open heart kits recalled for anesthetic quality issues
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- 2026-07-01FDA-DeviceMedlineClass INationwideMedline Convenience Kits recalled for anesthesia injection quality issues
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- 2026-07-01FDA-FoodCerelesClass INationwidePearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para Panqueques y Waffles) Net Wt 5.99 oz (170 g). Packed in 50 - 5.99 oz BOPP Pouch units per master case. Keep in a cool, dry place.
Undeclared allergens: Milk and Soy
- 2026-07-01FDA-FoodUtzClass IUtz Dirty chips recalled for Salmonella risk
Potential presence of Salmonella.
- 2026-07-01FDA-FoodUtzClass IUtz Zapp's Big Cheezy chips recalled for Salmonella risk
Potential presence of Salmonella.
- 2026-07-01FDA-FoodUtzClass IUtz Dirty Maui Onion Chips recalled for Salmonella risk
Potential presence of Salmonella.
- 2026-07-01FDA-FoodUtzClass IUtz Dirty Brand chips recalled for Salmonella risk
Potential presence of Salmonella.
- 2026-07-01FDA-FoodUtzClass IUtz Zapp's potato chips recalled for Salmonella risk
Potential presence of Salmonella.
- 2026-07-01FDA-FoodUtzClass IUtz Zapp's chips recalled for Salmonella risk
Potential presence of Salmonella.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry chocolate bars 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 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 chocolate bars 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 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
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