State

Oklahoma product recalls

73,738 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,040
Severe: 1,493
Most recent: 2026-10-28

Of the 5,822 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 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35576–35600 of 79560

SevereFDA (Devices)·Z-1770-2019·2019-07-17
Becton Dickinson Recalls Alaris Pump Infusion Sets Due to Occlusion Defect
Becton Dickinson is recalling Alaris Pump Infusion Sets because a wall thickness variation can cause incomplete occlusion, potentially leading to unintended or faster-than-expected medication delivery.
Product
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930, 11522558, 11607704, 10013361T, 2110-0500, 2126-0500, 2200-0500, 2411-0500, 2419-0007, 2420-0007, 2420-0500, 2421-0500, 2426-0007, 2426-0500, 2429-0500…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1847-2019·2019-07-17
GE Healthcare Recalls Panda Infant Radiant Warmers Due to Bedside Panel Cracking
GE Healthcare is recalling 28,094 Panda Infant Radiant Warmers because the bedside panels and latch areas can crack or break if the unit is moved using them instead of the designated handles.
Product
Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition to the external environment…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19E045000·2019-07-17
Reyco Fire Truck Front Suspension Recall for Shock Separation Risk
Reyco is recalling Fire Truck Independent Front Suspensions because front shocks may separate and damage the steering gear, potentially causing a loss of power steering assist.
Product
SUSPENSION:FRONT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1455-2019·2019-07-17
Teva Recalls Losartan Potassium Tablets Due to Impurity Detection
Teva Pharmaceuticals USA is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles, NDC 00591-3746-00
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1460-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active pharmaceutical ingredient.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1466-2019·2019-07-17
Major Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity
Major Pharmaceuticals is recalling Losartan Potassium 50 mg tablets because FDA testing found an impurity above acceptable levels.
Product
Losartan Potassium Tablets, USP. 50 mg. NDC# 0904-6390-61. Rx only. 100 count Unit Dose Cartons. Manufactured by Major Pharmaceuticals 17177 N. Laurel Park Drive Suite 233, Livonia, MI 48152.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1461-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1923-2019·2019-07-17
Philips HeartStart MRx Recall Due to AC Power Module Failure Risk
Philips is recalling HeartStart MRx devices used with specific AC power modules that may fail, potentially causing loss of power and failure to deliver shocks.
Product
Philips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1874-2019·2019-07-17
Hamilton Medical Recalls HAMILTON-G5 Ventilators Due to Ambient State Risk
Hamilton Medical is recalling 4,338 HAMILTON-G5 ventilators with software versions 2.60 or lower because they may enter an ambient state, requiring immediate alternative ventilation.
Product
HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for intensive care ventilation of adult and pediatric patients, and optionally infant and neonatal patients. The device is intended for use in the hospital and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1462-2019·2019-07-17
Losartan Potassium Tablets Recalled Due to Impurity Detection
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Product
Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1464-2019·2019-07-17
Losartan Potassium Tablets Recalled Due to Nitrosamine Impurity
Golden State Medical Supply is recalling Losartan Potassium 50 mg tablets because a nitrosamine impurity was detected in the active ingredient.
Product
Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1458-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1846-2019·2019-07-17
GE Healthcare Recalls Giraffe Infant Radiant Warmers Due to Panel Cracking
GE Healthcare is recalling 9,094 Giraffe Infant Radiant Warmers because bedside panels and latch areas can crack or break if the unit is moved using the panels instead of the designated handles.
Product
Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition to the external environment…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1456-2019·2019-07-17
Teva Recalls Losartan Potassium Tablets Due to Impurity Detection
Teva Pharmaceuticals is recalling Losartan Potassium 100 mg tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM 100 mg TABLET BULK 90 count bottles, NDC 00591-3747-00
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V535000·2019-07-17
Volkswagen Recalls 2015-2016 CC and Tiguan for Air Bag Defect
Volkswagen is recalling 27,822 2015-2016 CC and Tiguan vehicles because a defective air bag control unit may cause air bags to fail or deploy unexpectedly.
Product
VOLKSWAGEN — VOLKSWAGEN CC, TIGUAN
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1463-2019·2019-07-17
Losartan Potassium tablets recalled due to impurity detection
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Product
Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1959-2019·2019-07-17
Applied Medical Recalls Kii Fios First Entry Devices for Sterility Concerns
Applied Medical Resources Corp is recalling Kii Fios First Entry devices because they may not have met sterility requirements, potentially exposing patients to infectious agents.
Product
Kii Fios First Entry, 5 X 75 mm, RX only, REF CFF05 Qty: 6, Sterile R, Lot: 1330981, Exp: July 15, 2021, Applied Medical Resource Corp. Product Usage: Kii Fios first entry is indicated for use in general, abdominal, gynecological and thoracic minimally invasive surgical…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V534000·2019-07-17
Navistar Recalls 2020 IC CE School Buses Due to Electrical Overload
Navistar is recalling 2020 IC CE school buses because an electrical overload in the Body Control Module may cause the engine to start unexpectedly, increasing injury risk during service.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V533000·2019-07-17
Porsche Recalls 2016-2017 Models for Air Bag Control Module Defect
Porsche is recalling 2016-2017 911, Boxster, Cayman, and Panamera vehicles because a defective capacitor in the air bag control unit may cause air bags to fail or deploy unexpectedly.
Product
PORSCHE — PORSCHE 718 BOXSTER, PANAMERA, 911, 718 CAYMAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1457-2019·2019-07-17
Macleods Pharma Recalls Losartan Potassium Tablets Due to Impurity
Macleods Pharma USA Inc. is recalling Losartan Potassium tablets because an impurity was detected in the active ingredient.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1950-2019·2019-07-17
Helena Laboratories Recalls ColoCARE In-Vitro Diagnostic Kits
Helena Laboratories is recalling ColoCARE in-vitro diagnostic kits because the positive control failed to react appropriately in some tests.
Product
ColoCARE, Cat. No. 5651, packaged 50 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena Laboratories, Beaumont, TX.
Category
Medical Device
Distribution
34 states
HighCPSC·19169·2019-07-17
Bodum Bistro Toasters Recalled for Electric Shock Hazard
Bodum is recalling Bistro Toasters because they can leak electric current at maximum temperature, posing a shock hazard. No U.S. injuries were reported, but eight shocks occurred in Canada.
Product
Bodum Bistro Toasters
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1955-2019·2019-07-17
MAHURKAR and Argyle acute hemodialysis catheters recalled for inaccurate priming volume labels
COVIDIEN LLC is recalling MAHURKAR and Argyle acute hemodialysis catheters because the printed priming volume values are higher than the volumes required to fill each lumen.
Product
MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 8813793013 8813794005 8813794009 8813816005 8813816009 8813817005 8813817009 8815668007 8815668011 8815668021 8815668027 8817142005 8817143005 8817145005 8817146001 8817146007…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1958-2019·2019-07-17
Canon Radrex-i X-Ray System Software Malfunction Recall
Canon Medical System is recalling 46 Radrex-i X-Ray Systems due to a software malfunction that prevents image transmission from the wireless flat panel detector.
Product
Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software version: v5.00ER005 Product Usage: The RADREX-I is a general purpose x-ray system that employs Solid State Imager(s), SSXI, which converts x-rays directly into electrical signals which can, after…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1949-2019·2019-07-17
Helena Laboratories Recalls ColoCARE In-Vitro Diagnostic Kits
Helena Laboratories is recalling ColoCARE diagnostic kits because the positive control failed to react properly, potentially affecting test accuracy.
Product
ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena Laboratories, Beaumont, TX.
Category
Medical Device
Distribution
34 states