State
73,486 recalls have nationwide distribution and so reach Texas. 12,437 additional recalls listed Texas specifically in their distribution scope.
Of the 12,437 recalls naming Texas we have scored against our rubric, 1,720 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,926 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,437 recalls whose distribution notice names Texas specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Baxter Healthcare is recalling 498 units of MiniCap Extended Life PD Transfer Sets because they were distributed without FDA regulatory clearance. Affected units were distributed in 16 U.S. states.
Avanos Medical is recalling BALLARD Multi-Access Port Catheters because they were distributed with incorrect expiration dates on the packaging. The recall includes 6,280 devices.
Dr. Reddy's Laboratories is recalling 7,703 bottles of Lansoprazole Delayed-Release Capsules (30 mg, 90-count) nationwide due to failed dissolution specifications found during long-term stability testing.
ROi CPS LLC is recalling 1,750 Regard Custom Procedure Kits containing BD Luer Lok Access Devices distributed nationwide in Missouri.
Roche is recalling 14 Cobas Liat analyzer units due to detector noise causing false positive Influenza B results. Affected units were distributed in seven U.S. states and three countries.
Elmer Candy Corp is recalling Elmer's Pecan Egg candies due to pecan tree bark in the product. The recall affects 370,464 units from lot 2930 distributed in eight states.
Avanos Medical is recalling BALLARD Seal Cassette Replacement MAP catheter devices due to incorrect expiration dates on product labels. Affected lot 30143745 was distributed in the United States and internationally.
Microbiologics Inc recalls the Pneumonia (33 Targets) Control Panel due to a shelf-life discrepancy. The product's shelf-life was determined to be 6 months instead of the labeled 18 months.
Ansell is recalling Gammex Non-Latex PI Green surgical gloves (size 7 1/2) because the product was not submitted for required FDA inspection at the border. Distribution included Arizona, California, Nevada, Texas, Utah, and Washington.
Dr. Reddy's Laboratories is recalling 28,068 bottles of Atorvastatin Calcium 80 mg tablets nationwide due to failed impurity and degradation specifications. No illnesses or injuries have been reported.
Jaguar Land Rover is recalling 2016-2017 Range Rover and Range Rover Sport vehicles because the driver's seat belt retractor may not lock during hard braking.
Piaggio is recalling 2020-2021 MP3 500 scooters because zinc plating on brake hose fittings may contaminate brake fluid, reducing braking performance and increasing crash risk.
Mercedes-Benz is recalling 2021 S 500 and S 580 vehicles because an improperly secured steering column connector may disable safety features and gear shifts.
Autocar is recalling 2021-2022 XPEDITOR vehicles because the ABS modulation valve may be wired incorrectly, potentially extending braking distance and increasing crash risk.
Hyundai is recalling 2020 Accent vehicles with front seat belt pretensioners that may explode during a crash, projecting metal fragments that can strike and injure occupants.
Mercedes-Benz is recalling 2021-2022 Maybach S 580 vehicles because front seat trim parts may detach during rear air bag deployment, potentially causing improper air bag function and injury.
General Motors is recalling specific Truck Hero tonneau covers for 2019-2022 Chevrolet and GMC trucks because they may detach while driving, creating a road hazard.
General Motors is recalling certain 2020-2022 Chevrolet Traverse and 2021-2022 Buick Enclave vehicles because the harness connector to the roof rail air bags may have incompatible electrical terminals that could prevent air bag deployment in a crash.
Terex is recalling 2020-2022 XT Pro aerial devices because un lubricated pivot points may cause pins to seize and break retainers, risking boom failure.
Jayco is recalling 2022 White Hawk travel trailers because loose power inlet wiring may cause an electrical arc or short, increasing the risk of a fire.
SOUNDBOKS Inc. is recalling about 6,700 Gen. 3 Bluetooth speakers because the removable lithium-ion battery can overheat and pose a fire hazard. Consumers should stop using the speakers immediately and contact the company for a free replacement battery.
Keystone is recalling 2022 Alpine and related travel trailers due to power inlet lug bolts manufactured too hard to tighten properly, causing loose electrical connections that could lead to fire.
Maped Helix USA is recalling about 7,700 Helix Metal Lockable Drug Chests because the locking mechanism can fail, allowing unauthorized access to medications and posing a risk of poisoning.
Keystone is recalling 2019-2022 Cougar travel trailers due to improper outrigger clearance that may allow tires to contact the outrigger. Damaged tires can fail and cause loss of vehicle control and increased crash risk.
PlayMonster is recalling Kid O Hudson Glow Rattles because the rattle's legs can break off, posing a choking hazard to young children. The firm has received three reports of legs breaking off, though no injuries have been reported.