State

Oklahoma product recalls

73,596 recalls have nationwide distribution and so reach Oklahoma. 5,818 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,818
Critical: 1,040
Severe: 1,493
Most recent: 2026-10-14

Of the 5,818 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,818 recalls whose distribution notice names Oklahoma specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26876–26900 of 79414

HighFDA (Devices)·Z-1463-2021·2021-04-28
Biotronik Intica Neo 7 VR-T DX DF-1 ProMRI Recall for Battery Depletion
Biotronik is recalling 17 Intica Neo 7 VR-T DX DF-1 ProMRI implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI, REF 429559, UDI: 04035479156855 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2021·2021-04-28
Biotronik Iforia 7 ICDs Recalled for Premature Battery Depletion
Biotronik Inc is recalling 1,176 Iforia 7 implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK Iforia 7, vr-T, DX, DF-1,REF 390090, UDI: 04035479127176 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0437-2021·2021-04-28
Avanti Recalls 365 Whole Foods Market Farm Raised Cooked Shrimp
Avanti Frozen Foods is recalling 365 Whole Foods Market Farm Raised Cooked Shrimp because uncooked shrimp were inadvertently packaged as cooked.
Product
365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- to - Serve Tail-On/Peeled & Deveined/41-55 Shrimp/lb NET WT 32 OZ (2 LB) 907g packaged in clear plastic bag
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1443-2021·2021-04-28
Biotronik Ilestro 7 VR-T Defibrillators Recalled for Premature Battery Depletion
Biotronik Inc is recalling 1,000 Ilestro 7 VR-T implantable defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0454-2021·2021-04-28
Reser's Macaroni Salad Recalled for Undeclared Wheat and Egg Allergens
Reser's Fine Foods is recalling Freshness Guaranteed Macaroni Salad Amish because the bottom label incorrectly identifies the product as Red Potatoes or Baked Beans, failing to declare wheat and egg allergens.
Product
Freshness Guaranteed Macaroni Salad Amish, item # 579284, refrigerated, packaged in a clear cup with clear snap on lid, net wt. 32 oz. UPC 0 78742 13235 8. Each master case containing 6/32 oz. packages. Distributed by: Walmart Inc, Bentonville, AR. The CORRECT label is read…
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1475-2021·2021-04-28
Smiths Medical Recalls Medex High Pressure Adaptors and LogiCal Kits
Smiths Medical is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to potential manufacturing defects in welds.
Product
ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD, Model Number MX1030. for use during angiography and other special procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1442-2021·2021-04-28
Biotronik Ilestro 7 DR-T Recall for Premature Battery Depletion
Biotronik is recalling Ilestro 7 DR-T implantable defibrillators due to a potential for premature battery depletion. Affected devices are distributed nationwide and worldwide.
Product
BIOTRONIK Ilestro 7 DR-T, DF-4, REF383564, UDI: 04035479125202 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V301000·2021-04-28
Multiple Hyundai models recalled for engine piston ring defect
Hyundai is recalling 2019–2021 Kona, Elantra, and Veloster models with 2.0L engines. Improperly heat-treated piston rings may cause engine damage, stalling, and fire risk.
Product
HYUNDAI — HYUNDAI VELOSTER, ELANTRA, KONA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1453-2021·2021-04-28
BIOTRONIK IPERIA 7 ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling 2,881 IPERIA 7 ICDs and CRT-Ds due to a potential for premature battery depletion.
Product
BIOTRONIK IPERIA 7, DR-T DF4 ProMRI, REF 392423, UDI: 04035479128913 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V299000·2021-04-28
Suzuki Recalls 2019-2020 UH200 Motorcycles Due to Speedometer Defect
Suzuki is recalling 2019-2020 UH200 motorcycles because corroded speedometer resistors may cause the speedometer and odometer to stop working, increasing crash risk.
Product
SUZUKI — SUZUKI UH200
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1462-2021·2021-04-28
Biotronik ILIVIA Neo 7 VR-T DF-1 ProMRI Recall for Battery Depletion
Biotronik is recalling 74 ILIVIA Neo 7 VR-T DF-1 ProMRI implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI, REF 429531, UDI: 04035479156763 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1451-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 499 ITREVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ITREVIA 7, VR-T DF-1, REF 393040, UDI: 04035479129552 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2021·2021-04-28
Smiths Medical Recalls Medex High Pressure Adaptors and LogiCal Kits
Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to insufficient or incomplete welds.
Product
Mark 910 LogiCal, Model Number DPS567201. for blood pressure monitoring and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1454-2021·2021-04-28
Biotronik Inventa 7 ICDs Recalled for Premature Battery Depletion
Biotronik is recalling 702 Inventa 7 ICDs due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK INVENTRA 7, HF-T QP DF4 IS4, REF 393012, UDI: 04035479129286 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1455-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik Inc is recalling 658 ITREVIA 7 implantable defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ITREVIA 7, DR-T QP DF-1, REF 392412, UDI: 04035479128807 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21119·2021-04-28
Pentair Recalls StaRite and Mastertemp Pool Heaters Due to Fire Hazard
Pentair Water Pool and Spa is recalling about 4,700 StaRite and Mastertemp pool heaters because a connection can leak a combustible air-gas mixture, posing a fire hazard.
Product
StaRite and Mastertemp pool heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V298000·2021-04-28
2021 BMW 330E Seat Belt Buckle Assembly Bolt Not Properly Secured
BMW is recalling certain 2021 330E, 330i, M340i, and M3 vehicles due to an undertightened bolt on the front seat belt buckle assembly. The defect may prevent proper occupant restraint, increasing injury risk.
Product
BMW — BMW M340I, 330I, 330E, M3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V300000·2021-04-28
Blue Bird Recalls 2018-2021 School Buses for Power Steering Defect
Blue Bird is recalling 2018-2021 Vision and All American school buses because an electrical issue may cause a loss of power steering, increasing crash risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, ALL AMERICAN, VISION, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2021·2021-04-28
Smiths Medical Recalls Tubing Components Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of tubing components for blood-pressure transducers due to insufficient or incomplete welds.
Product
Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1449-2021·2021-04-28
BIOTRONIK IPERIA 7 ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling 3,832 IPERIA 7 ICDs and CRT-Ds due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK IPERIA 7,VR-T, DX, DF-1, ProMRI, REF 393032, UDI: 04035479129477 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1456-2021·2021-04-28
Biotronik ILIVIA 7 ICD Recall for Premature Battery Depletion
Biotronik is recalling 3,497 ILIVIA 7 implantable cardioverter defibrillators due to a potential for premature battery depletion. The recall covers units distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, DR-T DF4 ProMRI, REF 404623, UDI: 04035479142100 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2021·2021-04-28
Biotronik Iperia 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 1,652 Iperia 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK Iperia 7, DR-T, DF-1, ProMRI REF 392409, UDI: 04035479128777 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1441-2021·2021-04-28
BIOTRONIK Ilestro 7 DR-T ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling Ilestro 7 DR-T implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK Ilestro 7 DR-T, DF-1, REF383562, UDI: 04035479125189 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1478-2021·2021-04-28
Smiths Medical Recalls Medex High Pressure Tubing Due to Weld Defects
Smiths Medical ASD Inc. is recalling specific lots of Medex high pressure tubing and components due to insufficient or incomplete welds.
Product
HIGH PRESSURE TUBING, 72IN, Model Number MX152114 (Component). Stopcocks and manifolds are used to control the direction of IV fluid flow.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2021·2021-04-28
Smiths Medical Recalls LogiCal Monitoring Sets Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of LogiCal Monitoring Sets and related components due to insufficient or incomplete welds.
Product
LogiCal Monitoring Set, Model Number DPS564898. for blood pressure monitoring and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide