State

Oklahoma product recalls

73,827 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,823
Critical: 1,040
Severe: 1,494
Most recent: 2026-11-04

Of the 5,823 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 1,494 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54301–54325 of 79650

HighFDA (Devices)·Z-0727-2016·2016-02-10
Philips INTEGRIS Allura X-ray Systems Recalled for Image Display Error
Philips is recalling INTEGRIS Allura X-ray systems because a software error may cause still images to be displayed as live images, potentially leading to misinterpretation.
Product
INTEGRIS Allura 15-12 (mono); Model Number: 722043 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0711-2016·2016-02-10
Philips Recalls Allura Xper FD20 Biplane Systems Due to Image Display Error
Philips is recalling Allura Xper FD20 Biplane systems because a software issue may cause still images to be misinterpreted as live images.
Product
Allura Xper FD20 Biplane; Model Numbers: 722013 722008 722015 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional procedures. This includes, e.g. peripheral, cerebral, thoracic and abdominal angiography, as well as PTCAs, stent…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0703-2016·2016-02-10
Philips Allura Xper X-ray Systems Recalled for Image Display Error
Philips is recalling Allura Xper FD10/10 systems because a software issue may cause still images to be mistaken for live images during X-ray procedures.
Product
Allura Xper FD10/10; Model Numbers: 722027 722011 722005 Intended for Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and ElectroPhysiology (EP).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0746-2016·2016-02-10
Resmed Recalls Astral 100 and 150 External Batteries Due to Start-Up Issue
Resmed Corporation is recalling Astral 100 and 150 external batteries because of a start-up issue. The recall affects 14,736 units distributed in the US and internationally.
Product
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for example, the largest population of patients on the Astral device is COPD patients primarily using the device at night with some daytime use for recovery…
Category
Medical Device
Distribution
32 states
HighFDA (Devices)·Z-0721-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be mistaken for live images.
Product
INTEGRIS V3000; Model Number: 72243, 72244, 72245 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0716-2016·2016-02-10
Philips Allura Centron Medical Imaging System Recalled for Image Display Error
Philips is recalling Allura Centron systems because a software error may cause still images to be misinterpreted as live images during medical procedures.
Product
Cardiovascular Allura Centron; Model Number: 722400 The Allura CV2O is intended for physicians (e.g. cardiologists and radiologists), assisted by trained hospital staff (e.g. nurses and lab technicians), who are qualified to perform medical procedures on humans (having a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0734-2016·2016-02-10
Owens & Minor Recalls MediChoice Cohesive Bandages Due to Microbial Contamination
Owens & Minor is recalling MediChoice sterile cohesive bandages because testing revealed microbial contamination. The affected bandages were distributed nationwide.
Product
MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] General Hospital Use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0748-2016·2016-02-10
Radiometer AQURE System Recalled for Sample Type Design Error
Radiometer America Inc is recalling 375 AQURE Systems (Model 933-599) because a design error may leave the sample type field blank, potentially leading to misinterpretation of blood gas and immunoassay results.
Product
AQURE System; Model Number: 933-599. The AQURE System manages blood gas and immunoassay analyzers.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V080000·2016-02-10
Thomas Built Buses Recall School Buses with Peeling Stop Arm Decals
Daimler Trucks North America is recalling 878 school buses because reflective decals on stop arms may peel off, reducing visibility and increasing crash risk.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, MINOTOUR, SAF-T-LINER HDX, SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V076000·2016-02-10
Ram ProMaster Vans Recalled for Electronic Stability Control Defect
Chrysler is recalling 2016 Ram ProMaster vans with 3.0L diesel engines because the Electronic Stability Control system may fail to reactivate after being disabled, increasing crash risk.
Product
RAM — RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0709-2016·2016-02-10
Philips UNIQ and Allura Systems Recall for Image Interpretation Error
Philips is recalling UNIQ and Allura systems because a software issue may cause still images to be misinterpreted as live images during medical procedures.
Product
UNIQ FD OR table; Model Number 722035 The Philips UNIQ is intended for use on human patients to perform: " Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0705-2016·2016-02-10
Philips Allura Xper FD20/10 Recalled for Image Display Error
Philips is recalling 13,297 Allura Xper FD20/10 systems because a software error may cause still images to be interpreted as live images.
Product
Allura Xper FD20/10; Model Numbers: 722029 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional procedures. This includes, e.g. peripheral, cerebral, thoracic and abdominal angiography, as well as PTCAs, stent placements…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0730-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be mistaken for live images.
Product
INTEGRIS BV3000 MONO; Model Number: 72241 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V075000·2016-02-10
Toyota Recalls 2013-2016 Scion FR-S for Ignition Key Removal Defect
Toyota is recalling 2013-2016 Scion FR-S vehicles because the ignition key may be removed without the transmission in Park, increasing the risk of the vehicle rolling away.
Product
SCION — SCION FR-S
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0726-2016·2016-02-10
Philips INTEGRIS Allura 9 Biplane Recalled for Image Interpretation Risk
Philips is recalling INTEGRIS Allura 9 Biplane systems because still images may be misinterpreted as live images, posing a risk to patient safety.
Product
INTEGRIS Allura 9 (biplane); Model Number: 722021 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0702-2016·2016-02-10
Philips Allura Xper X-ray Systems Recalled for Image Interpretation Error
Philips is recalling Allura Xper FD10 systems because a software defect may cause still images to be mistaken for live images during cardiovascular procedures.
Product
Allura Xper FD10, FD10 C, and FD10 F; Model Numbers: 722026 722010 722003 722002 722001 Intended for Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0704-2016·2016-02-10
Philips Allura Xper OR Table Recall for Image Interpretation Error
Philips is recalling Allura Xper FD10 OR Tables because still images may be misinterpreted as live images during cardiovascular procedures.
Product
Allura Xper FD10 OR Table; Model Numbers: 722033 722022 Intended for Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and ElectroPhysiology (EP).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0747-2016·2016-02-10
Synthes Small Electric Drive Recalled for Malfunction and Unintended Operation
The Anspach Effort, Inc. is recalling 599 Synthes Small Electric Drive units because they may malfunction, fail to operate, or start unintentionally.
Product
Synthes Small Electric Drive (SED). For use in general traumatology.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0719-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be mistaken for live images.
Product
INTEGRIS BN/BV3000; Model Number: 72240 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0713-2016·2016-02-10
Philips Allura Xper FD20/20 Recall for Image Interpretation Error
Philips is recalling 13,297 Allura Xper FD20/20 systems because a software issue may cause still images to be mistaken for live images during medical procedures.
Product
Allura Xper FD20/20; Model Number: 722038 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional procedures. This includes, e.g. peripheral, cerebral, thoracic and abdominal angiography, as well as PTCAs, stent placements…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0708-2016·2016-02-10
Philips UNIQ and Allura Systems Recalled for Image Interpretation Error
Philips is recalling UNIQ and Allura imaging systems because still images may be misinterpreted as live images during medical procedures.
Product
UNIQ FD; Model Numbers: 722028 The Philips UNIQ is intended for use on human patients to perform: " Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0729-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura systems because a software issue may cause still images to be mistaken for live images.
Product
INTEGRIS CV; Model Number: 722030 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and interventional…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0725-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be misinterpreted as live images.
Product
INTEGRIS BV5000: Model Number: 72249 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0723-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura systems because a software issue may cause still images to be mistaken for live images during procedures.
Product
INTEGRIS BH5000; Model Number: 72247 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0510-2016·2016-02-10
This Kid Saves Lives Chocolate Chip Bars Recalled for Undeclared Milk
This Bar Saves Lives is recalling This Kid Saves Lives Chocolate Chip bars because they contain whey protein but do not identify milk on the label.
Product
This Kid Saves Lives Chocolate Chip UPC #10858497004097 UPC# 858497004090
Category
Food
Distribution
28 states