State
72,992 recalls have nationwide distribution and so reach Oklahoma. 5,788 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,788 recalls naming Oklahoma we have scored against our rubric, 1,033 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,238 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,788 recalls whose distribution notice names Oklahoma specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BD Recon LT avalanche transceivers are recalled because the switch mechanism can corrode and fail, potentially preventing rescuers from locating avalanche victims. Six devices have malfunctioned; no injuries reported.
Jayco is recalling specific 2024 and 2025 motorhomes because incorrect Federal labels may allow the vehicles to be overloaded, increasing crash risk.
General Motors is recalling certain 2019–2022 Cadillac and Chevrolet vehicles with 10-speed transmissions due to internal transmission damage that may cause wheel lock-up while driving.
INEOS is recalling certain 2024 Grenadier vehicles because the door button mechanism may lack sufficient grease, preventing the door from fully latching. An unlatched door can open unexpectedly while driving, increasing injury risk.
Nestlé-USA is recalling all lots of Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Strawberry Apple flavor following complaints of infant choking. The product was distributed across 42 states and Puerto Rico.
Airstream is recalling certain Classic travel trailers because the sofa footrest switch wiring may overheat, increasing the risk of a fire.
Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Banana flavor are recalled nationwide due to complaints of infant choking. All lots in both 1.59 oz and 3.2 oz packages are affected.
The PENTAX Medical Video Colonoscope (Model EC38-i20cL) can develop excessive heat at the tip during procedures, potentially causing thermal burns to patient tissue. Users reported dark images and steam-like smoke from the device.
OCBW INC is recalling Beverage Base Sweet&Sour in 3-gallon bulk containers due to undeclared Yellow #5, a color additive. The product was distributed across eight states and poses a risk to consumers with sensitivities to this ingredient.
GE Healthcare's Optima MR360 MRI systems may allow unsafe RF energy exposure if a scan resumes after power loss. The user interface can incorrectly enable scanning when tissue-heating levels exceed safe limits.
CareFusion is recalling BD Pyxis MedBank medication management cabinets due to inadequate labeling. A contraindication statement must be added to warn against use in procedure and operating rooms.
A software bug in IntelePACS causes incorrect diagnostic value calculations on Daylight Saving Time transition dates, risking incorrect patient diagnoses.
Tyber Medical is recalling A.L.P.S. mvX Medial Tibia Plates because the locking screw may pass through the locking hole during surgery instead of securing properly, causing surgical delays. The recall affects 210 units distributed nationwide.
Tyber Medical is recalling A.L.P.S. mvX Anatomic Lateral Fibula Plates due to locking screw passing through the locking hole intra-operatively, causing surgical delays. The recall affects 397 units distributed nationwide.
Pentax of America is recalling 138 PENTAX Medical Video Upper GI Scopes due to a thermal injury risk. The light guide tip can become excessively hot during endoscopic procedures, potentially burning patient tissue.
A software issue in the Leica Biosystems CM1950 cryostat firmware update could result in loss of patient tissue. Serial numbers 12835 and 12854 are affected.
Tyber Medical is recalling A.L.P.S. mvX Anatomic Lateral Fibula Plates nationwide due to reports that locking screws may pass through the locking hole during surgery, causing surgical delays.
Padagis US LLC recalls Estradiol Gel 0.1% nationwide due to defective packets that may not be fully sealed, potentially allowing ethanol loss.
Pentax EPK-i8020c video processors can overheat during endoscopic procedures, creating a risk of thermal burns to patient tissues. The light guide tip becomes hot and may cause injury to mucous membranes.
Tyber Medical is recalling A.L.P.S. mvX Anatomic Lateral Fibula Plates (418 units, nationwide) because the locking screw may pass through the locking hole during surgery, causing surgical delays.
Tyber Medical is recalling A.L.P.S. mvX-P Anatomic Lateral Fibula Plates because the locking screw may pass through the locking hole during surgery, causing surgical delays.
Tyber Medical is recalling 115 A.L.P.S. mvX orthopedic plates because the locking screw can pass through the locking hole during surgery, causing surgical delays and inadequate fracture fixation.
A software issue in the DxC 500 AU analyzer prevents correct tracking of assay expiration dates after software upgrades. Expired assays may be used, potentially producing inaccurate patient test results.
Scientia Vascular is recalling 120 Socrates 38 Aspiration Catheters due to manufacturing defects that created channels in the packaging seal. The defect could potentially compromise the sterile barrier on devices used for acute stroke treatment.
BD Alaris Pump Module user manual incorrectly instructs users to leave the safety clamp open when reloading infusion sets, potentially causing accidental over-infusion.