State
72,982 recalls have nationwide distribution and so reach Texas. 12,390 additional recalls listed Texas specifically in their distribution scope.
Of the 12,390 recalls naming Texas we have scored against our rubric, 1,705 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,407 (19%) are Severe.
Which agencies issued them
These figures cover only the 12,390 recalls whose distribution notice names Texas specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dearlomum retractable mesh safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor. About 2,200 units are affected.
WLIVE Fabric 15-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the federal standard under the STURDY Act. About 6,600 units affected.
SPPTTY kids 14- and 18-inch bicycles are being recalled because multiple components contain lead exceeding the federal lead content ban. About 200 units are affected.
Creekliybear "Pack and Play" aftermarket play yard mattresses are being recalled because they exceed thickness requirements and may not fit certain play yards. About 21,500 units affected.
Unbranded braided crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct breathing. About 260 units are affected.
Momentum Vida E+ e-bikes are being recalled because the fork steerer tube can crack, break or separate during use, posing a fall hazard. About 6,200 units are affected.
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.
Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Philips Respironics is recalling BiPAP A30 and BiPAP Hybrid A30 ventilators. The devices do not have an indication for use in patients with respiratory failure.
Hardy Diagnostics is recalling HardyCHROM CRE culture medium (Catalog No. G323) distributed across 22 US states and Puerto Rico. The product failed quality control testing due to breakthrough growth of Klebsiella pneumoniae.
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Cucumbers sold in 40 lb boxes are being recalled because they have the potential to be contaminated with Salmonella. 71 cases are affected.
The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.
Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.
The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.
Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.
Philips Ultrasound is recalling Philips S5-1 Transducers because they were refurbished beyond their useful life, which may affect device performance and safety.
Preservative-free Lidocaine HCl Injection 1%, compounded by Medivant Healthcare, is being recalled for lack of assurance of sterility. 29,700 vials are affected.
Ketamine Hydrochloride Injection 500 mg/5 mL multi-dose vials compounded by Medivant Healthcare are being recalled for lack of assurance of sterility. 14,725 vials are affected.