Go Backs

Oklahoma Recalls

13,439 recalls distributed in Oklahoma

per page
Hetero Labs Limited (Unit V)
Medium RiskFDA Drug

Camber Pharmaceuticals Pantoprazole Sodium Tablets Recalled for Discoloration

  • Distributed nationwide
  • Sold at Camber Pharmaceuticals, Inc.
Recalled
Added
Medium RiskNHTSA

Weldon Akron Brass PowerView 700 Displays Recalled for Failure Risk

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added
Bentley Motors
Medium RiskNHTSA

2026 Bentley Bentayga Recalled for Incorrect Weight Capacity Labels

  • Distributed nationwide
  • Sold at Authorized Bentley Dealers
Recalled
Added
Ford Motor
Medium RiskNHTSA

2015-2017 Ford F-150 Recalled for Unexpected Downshifting

  • Distributed nationwide
  • Sold at Ford dealers
  • 1,392,935 units affected
Recalled
Added
Winnebago Industries
Medium RiskNHTSA

2026-2027 Winnebago Suncruiser and Sunflyer Recalled for Missing Reflectors

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added
The Harvard Drug
Medium RiskFDA Drug

Memantine Hydrochloride Extended-Release Recalled for Dissolution Failure

  • Distributed nationwide
  • Sold at Major Pharmaceuticals
Updated
Recalled
Critical RiskFDA Device

Siemens MAGNETOM and Biograph MRI Systems Recalled for Helium Leak Risk

  • Distributed nationwide
  • Sold at authorized medical distributors, specialty retailers
  • Helium gas contamination
Updated
Recalled
Medium RiskFDA Device

ARTIS Pheno Systems Recalled for Unintentional Radiation Exposure Risk

  • Distributed nationwide
  • Sold at Siemens Medical Solutions USA, Inc.
Recalled
Added
THERAKOS DEVELOPMENT
Medium RiskFDA Device

Cellex Photopheresis Kit Recalled for Centrifuge Bowl Dislodgment Risk

  • Distributed nationwide
  • Sold at Specialty medical distributors, Direct to healthcare facilities
Recalled
Added
B Braun Medical
Critical RiskFDA Device

B. Braun Hemodialysis Bloodlines Recalled for Air Bubble Risk

  • Distributed nationwide
  • Sold at Medical distributors, Dialysis centers
  • 7,324,458 units affected
Recalled
Added
Chrysler (FCA US, LLC)
Medium RiskNHTSA

2026 Jeep Cherokee Recalled for Brake Module Failure

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added
Chrysler (FCA US, LLC)
Medium RiskNHTSA

2026 Jeep Wrangler Recalled for Insufficient Child Seat Tether Welds

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added
Chrysler (FCA US, LLC)
Medium RiskNHTSA

2025-2026 Ram Pickup and Cab Chassis Recalled for Instrument Panel Failure

  • Distributed nationwide
  • Sold at Authorized dealers
  • 65,348 units affected
Recalled
Added
Medium RiskNHTSA

2018-2022 Honda Odyssey Recalled for Unexpected Air Bag Deployment

  • Distributed nationwide
  • Sold at authorized Honda dealers
  • 440,830 units affected
Recalled
Added
Jayco
Medium RiskNHTSA

2025-2026 Entegra Ethos RVs Recalled for Incorrect Seating Capacity Labels

  • Distributed nationwide
  • Sold at authorized Jayco dealers
Recalled
Added
Pierce Manufacturing
Medium RiskNHTSA

2015-2026 Pierce Aerial Firetrucks Recalled for Faulty Outrigger Indicator Lights

  • Distributed nationwide
  • Sold at Authorized Pierce dealers
Recalled
Added
Daimler Trucks North America
High RiskNHTSA

2024-2027 Thomas Built Buses Saf-T-Liner C2 Recalled for Lighting Defect

  • Distributed nationwide
  • Sold at Authorized Daimler Trucks North America dealers
Recalled
Added
Hyundai Motor America
Medium RiskNHTSA

2021-2026 Genesis GV70, G90, G80, and GV80 Recalled for Fuel Leak and Fire Risk

  • Distributed nationwide
  • Sold at Genesis authorized dealers
  • 94,760 units affected
Recalled
Added
Kia America
High RiskNHTSA

2022-2026 Kia Carnival Recalled for Fuel Leak and Fire Risk

  • Distributed nationwide
  • Sold at authorized Kia dealers
  • 141,032 units affected
Recalled
Added
Harley-Davidson Motor
High RiskNHTSA

2025-2026 Harley-Davidson Softail Motorcycles Recalled for Rear Brake Loss

  • Distributed nationwide
  • Sold at Authorized Harley-Davidson Dealers
  • 16,994 units affected
Recalled
Added
Remel
Medium RiskFDA Device

Remel Yeastone Broth Recalled Due to Potential Incorrect Antifungal Results

  • Distributed nationwide
  • Sold at Direct distribution to laboratories and healthcare facilities
Recalled
Added
Insulet
Critical RiskFDA Device

Omnipod 5 Pods Recalled for Insulin Leak and Under-Delivery Risk

  • Distributed nationwide
  • Sold at Authorized medical distributors, Pharmacies
  • 1,240,115 units affected
Recalled
Added
Medium RiskFDA Device

Philips AneurysmFlow Software Recalled for Unreliable Prognostic Data

  • Distributed nationwide
  • Sold at Philips Medical Systems, Authorized Medical Device Distributors
Recalled
Added
High RiskFDA Device

Arjo Tenor Mobile Patient Lifts Recalled for Falling Hazard

  • Distributed nationwide
  • Sold at Authorized Medical Device Distributors
Recalled
Added