State

Oklahoma product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42126–42150 of 79629

HighFDA (Devices)·Z-1433-2018·2018-04-25
Philips Intera 1.5T MRI Systems Recalled for Helium Gas Risk
Philips is recalling Intera 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.
Product
Intera 1.5T; 1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T Master/Nova Model 781106, 4) Intera 1.5T Master CV Model 781107, 5) Intera 1.5T Explorer/ Nova Dual Model 781108, 6) Intera 1.5T IT Model 781160, 7) Intera 1.5T…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1378-2018·2018-04-25
Cook Inc. Recalls MINC Benchtop Incubators Due to Temperature Control Defect
Cook Inc. is recalling 4,451 MINC Benchtop Incubators because a heater defect may cause temperatures to become too high or too low for proper cell culture.
Product
MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a microprocessor controlled, gassed, humidified, incubator intended for use in cell culture.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1414-2018·2018-04-25
Philips IQon Spectral CT Recalled for Emergency Stop Defect
Philips is recalling 47 IQon Spectral CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.
Product
IQon Spectral CT - Model no. 728332, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1107-2018·2018-04-25
Hungry Jack Pancake and Waffle Mix Recalled for Salmonella
The J.M. Smucker Company is recalling Hungry Jack Original Pancake & Waffle Mix because the product tested positive for salmonella.
Product
HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
Category
Food
Distribution
25 states
HighFDA (Devices)·Z-1401-2018·2018-04-25
Siemens Oncor Impression Plus Linear Accelerator Software Recall
Siemens is recalling 15 Oncor Impression Plus linear accelerators to update software and reduce the risk of collision during automated cancer treatments.
Product
ONCOR Impression Plus, Digital Linear Accelerator, Model No. 05857912 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1389-2018·2018-04-25
Stryker Power-LOAD Cot Fastening System Recalled for Broken Floor Plates
Stryker is recalling 4,724 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.
Product
Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and unloading of a compatible wheeled stretcher (ambulance cot) to and from a transport vehicle and to secure the ambulance cot during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1410-2018·2018-04-25
Philips CT Scanner Recall Due to Emergency Stop Defect
Philips is recalling 106 Brilliance Big Bore CT scanners because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading or unloading.
Product
Brilliance Big Bore (Oncology) - Model no. 728243, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1402-2018·2018-04-25
Siemens PRIMUS HI Digital Linear Accelerator Software Recall
Siemens is recalling 18 PRIMUS HI Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.
Product
PRIMUS HI, Digital Linear Accelerator, Model No. 04504200 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1431-2018·2018-04-25
Philips Intera 0.5T MRI Recalled for Helium Gas Risk
Philips is recalling 8,205 Intera 0.5T MRI scanners worldwide due to a potential risk of helium gas release during a magnet quench.
Product
Intera 0.5T Standard, Model 781101 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1406-2018·2018-04-25
Philips Ingenuity Core CT Systems Recalled for Couch Movement Hazard
Philips is recalling 281 Ingenuity Core CT systems because the emergency stop may fail to lock the couch, allowing it to move during patient loading.
Product
Ingenuity Core - Model no. 728321, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1381-2018·2018-04-25
Zimmer Biomet Recalls Segmental System Proximal Femoral Components
Zimmer Biomet is recalling specific proximal femoral components due to potential machining debris that may not have been adequately removed during cleaning.
Product
Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is used for solving complex salvage cases to address patients with severe bone loss associated with disease, trauma, or revision.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1397-2018·2018-04-25
Siemens MEVATRON M2 Linear Accelerator Recalled for Collision Risk
Siemens is recalling 18 MEVATRON M2 linear accelerators to update software and reduce the risk of collision during automated cancer treatments.
Product
MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1442-2018·2018-04-25
Philips T5 MRI Scanner Recalled for Helium Gas Risk
Philips is recalling T5 MRI scanners due to a potential risk of helium gas release during a magnet quench.
Product
T5 Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1428-2018·2018-04-25
Halyard Closed Suction System Flex Connectors May Disconnect During Use
Halyard Health is recalling certain Closed Suction Systems because Flex Connectors may become loose or disconnect before or during use.
Product
Halyard Closed Suction System for Adults, Turbo- cleaning¿Closed¿Suction¿System¿for¿Adults,¿Double¿Swivel¿Elbow (DSE). Used to aspirate liquids or semisolids from a patient's upper airway. a. HALYARD* TURBO-CLEANING 14FR DSE 21.3IN/54 CM (GREEN); b. HALYARD* TRACH…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18739·2018-04-25
HD Supply Recalls Seasons Ceiling Fans Due to Impact Hazard
HD Supply is recalling Seasons ceiling fans because brackets can break, causing blades to fall. No injuries have been reported, but one instance of minor property damage occurred.
Product
Seasons ceiling fans
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1400-2018·2018-04-25
Siemens ONCOR Impression Linear Accelerator Software Update Recall
Siemens is recalling seven ONCOR Impression Digital Linear Accelerators to update software and reduce the risk of collision during automated cancer treatments.
Product
ONCOR Impression , Digital Linear Accelerator, Model No. 05857920 Product Usage: The intended use of the device is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1435-2018·2018-04-25
Philips Achieva 1.5T MRI Systems Recalled for Helium Gas Risk
Philips is recalling 8,205 Achieva 1.5T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Product
Achieva 1.5T: 1) Nova (Dual), Model 781173, 2) Achieva 1.5T Initial Systems Model 781178, 3) Achieva 1.5T Nova Model 781196, 4) Achieva 1.5T Conversion Model 781283, 5) Achieva 1.5T Model 781296, 6) Achieva 1.5T R5 based Model 781343, 7) Achieva 1.5T Conversion R5 based Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1439-2018·2018-04-25
Philips ACS-NT MRI Scanner Recalled for Helium Gas Leak Risk
Philips is recalling 8,205 ACS-NT MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Product
ACS-NT, Model 78108 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1403-2018·2018-04-25
Teleflex Medical One Way Valve Recall for Potential Disconnection
Teleflex Medical is recalling specific lots of HUDSON RCI One Way Valves because they may disconnect, causing an interruption of ventilation to patients.
Product
Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in respiratory and anesthesia circuits to connect two or more components of a breathing system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1408-2018·2018-04-25
Philips Brilliance iCT CT Systems Recalled for Emergency Stop Defect
Philips is recalling 295 Brilliance iCT CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.
Product
Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0633-2018·2018-04-25
AvKARE Recalls Amantadine HCl Capsules for Dissolution Failure
AvKARE Inc. is recalling 2,135 cartons of Amantadine HCl Capsules, 100 mg, because the product failed dissolution specifications.
Product
AMANTADINE HCL — AMANTADINE HCL (AMANTADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1385-2018·2018-04-25
Datascope Mega Intra-Aortic Balloon Catheter Recalled for Missing Contraindications
Datascope is recalling Mega Intra-Aortic Balloon Catheters because the U.S. Instructions for Use were missing the Contraindications section.
Product
Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic balloon catheter and accessories are used to provide counter pulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the heart…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1114-2018·2018-04-25
Swire Coca Cola Recalls Diet Dr Pepper Bottles for Foreign Material
Swire Coca Cola is recalling 366 cases of Dr. Pepper Est. 1885 Diet, 20 FL Oz bottles due to the potential presence of foreign material.
Product
Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1422-2018·2018-04-25
Carefusion Recalls Jamshidi Needle Biopsy Devices Due to Packaging Integrity Concerns
Carefusion 2200 Inc is recalling 790 units of Jamshidi Needle Biopsy devices because the integrity of the sterile packaging is potentially compromised.
Product
JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP, 16G X 100MM DISP, 17G X 100MM, 16G X 70MM DISP]; STERILE;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1416-2018·2018-04-25
Terumo HX2 Temperature Management System Recall for Updated Cleaning Instructions
Terumo is recalling HX2 Temperature Management Systems to update cooler-heater cleaning instructions. The recall affects 2,393 units distributed worldwide.
Product
Terumo HX2 Temperature Management System, Catalog No. 809810 The Terumo HX2 Temperature Management System is indicated for use to supply temperature regulated water to heat exchangers during open heart surgery.
Category
Medical Device
Distribution
Distributed nationwide