State
72,913 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.
Of the 13,245 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,843 (21%) are Severe.
Which agencies issued them
These figures cover only the 13,245 recalls whose distribution notice names California specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Loard's Ube Ice Cream in 32 oz tubs is being recalled because milk, Red #3, Red #40, Blue #1 and Blue #2 are undeclared on the label. 1,568 units are affected.
Loard's Almond Joy Ice Cream in 32 oz tubs is being recalled because milk, almonds, soy and sulfites are undeclared on the label. 100 units are affected.
Medline is recalling certain Dental Pack and Surgical Pack convenience kits due to calibration issues with sterilization equipment that may affect sterility assurance. Approximately 3,508 units were distributed nationwide.
Loard's Lime Sherbert in 32 oz tubs is being recalled because milk, wheat, soy, Yellow #5 and Green #3 are undeclared on the label. 110 units are affected.
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.
Loard's Peppermint Ice Cream in 32 oz and 56 oz tubs is being recalled because milk, soy and Red #40 are undeclared on the label.
Medline Industries is recalling eight models of Convenience Kits due to calibration issues with sterilization equipment that may have affected the sterility assurance level of the devices.
Loard's Blueberry Cheesecake Ice Cream in 32 oz tubs is being recalled because milk, Red #40 and Blue #1 are undeclared on the label. 200 units are affected.
Loard's Coconut Pineapple Ice Cream in 32 oz and 56 oz tubs is being recalled because milk is undeclared on the label.
Loard's Black Raspberry Ice Cream in 32 oz tubs is being recalled because milk, Red #40 and Blue #1 are undeclared on the label. 446 units are affected.
Loard's Sea Salt Caramel Ice Cream in 32 oz tubs is being recalled because milk, soy and sulfites are undeclared on the label. 1,064 units are affected.
Silver Moon LP dba Loard's Ice Cream is voluntarily recalling Loard's Chocolate Marble Ice Cream (32 oz) because it contains undeclared milk.
Loard's Burgundy Cherry Ice Cream in 32 oz tubs is being recalled because milk, Red #40, Blue #1 and Blue #2 are undeclared on the label. 618 units are affected.
Loard's Butter Brickle Ice Cream in 32 oz tubs is being recalled because milk, almonds and soy are undeclared on the label. 556 units are affected.
Chocolate Showers Ice Cream, sold under five store labels, is being recalled because soy is undeclared on the label. 1,396 units are affected.
Loard's Brownie Nut Fudge Ice Cream in 32 oz tubs is being recalled because milk, walnuts, eggs, wheat and soy are undeclared on the label. 78 units are affected.
Loard's Raspberry Sherbert in 32 oz tubs is being recalled because milk and Red #40 are undeclared on the label. 132 units are affected.
Loard's Banana Ice Cream in 32 oz and 56 oz tubs is being recalled because milk and Yellow #5 are undeclared on the label.
Medline is recalling Convenience Kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the products.
Peppermint Ice Cream sold under four store labels is being recalled because it contains undeclared Red #40. 1,076 units are affected.
Medline Industries is recalling multiple convenience kits due to calibration issues with sterilization and packaging equipment that may compromise sterility assurance. Approximately 5,497 units were affected and distributed nationwide.
DFI Co., Ltd. is recalling the One Step UTI in vitro diagnostic test (REF: 3374) because it was distributed without required FDA premarket clearance or approval.
Spacelabs Healthcare is recalling 57 SL Command Module (Model 91496) patient monitoring devices due to a manufacturing issue with the electrical leakage tester that could affect device safety and performance.
DFI Co., Ltd. is recalling One Step K in vitro diagnostic test devices (761 units) because they were distributed without required FDA premarket clearance or approval.
Orthorebirth Co Ltd is recalling ZENBONE resorbable bone void filler because the product falls outside standard specifications. The recall affects specific lot numbers distributed nationwide in California and Florida.