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.

41901–41925 of 79629

CriticalFDA (Food)·F-1477-2018·2018-05-09
Viable Solutions Recalls Mitragyna Speciosa Leaf Powder Due to Salmonella Risk
Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder (Green Horn) sold as Herbal-Salvation.com due to potential Salmonella contamination.
Product
Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0703-2018·2018-05-09
AuroMedics Recalls Linezolid Injection Bags Due to Sterility Concerns
AuroMedics Pharma LLC is recalling Linezolid Injection bags due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
Product
LINEZOLID — LINEZOLID (LINEZOLID)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0705-2018·2018-05-09
AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns
AuroMedics Pharma LLC is recalling 261,250 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0709-2018·2018-05-09
AuroMedics Recalls Levofloxacin IV Bags Due to Sterility Concerns
AuroMedics Pharma LLC is recalling 308,112 bags of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of mold.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1603-2018·2018-05-09
Philips MultiDim Eleva Imaging System Recalled for Uncontrolled Table Rotation
Philips is recalling 184 MultiDim Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Product
MultiDim Eleva 708032 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1605-2018·2018-05-09
Philips MultiDiagnost Eleva Imaging System Recalled for Uncontrolled Table Rotation
Philips is recalling 37 MultiDiagnost Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Product
MultiDiagnost Eleva 708036 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0706-2018·2018-05-09
AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns
AuroMedics Pharma LLC is recalling Levetiracetam Injection due to a lack of assurance of sterility and a confirmed report of leaking bags and mold.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1607-2018·2018-05-09
Philips MD-Eleva Medical Imaging System Recalled for Tilt Actuator Failure
Philips is recalling 199 MD-Eleva imaging systems because a tilt actuator may break, causing the table to rotate uncontrollably at high speed.
Product
Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1606-2018·2018-05-09
Philips MD-Eleva Imaging System Recalled for Uncontrolled Table Rotation
Philips is recalling 206 MD-Eleva imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Product
Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1538-2018·2018-05-09
Zimmer Biomet Recalls Modular Hip Head Components Due to Sizing Errors
Zimmer Biomet is recalling 18 modular hip head components because two lots of different sizes were potentially commingled. This may lead to the use of an incorrect sized head.
Product
Modular Head Component, Biomet Hip System; Item No. 11-363661, Hip Joint, metal/polymer/metal, semi-constrained, porous-coated, uncemented prosthesis The device is used in treatment of patients who need total hip arthroplasty, and consists of modular components and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0804-2018·2018-05-09
Sanofi Recalls Over-Concentrated Docetaxel Injection Vials Nationwide
Sanofi-Aventis is recalling 19,580 vials of Docetaxel injection concentrate due to potential over-concentration. The affected lots were distributed nationwide.
Product
DOCETAXEL — DOCETAXEL (DOCETAXEL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0704-2018·2018-05-09
AuroMedics Recalls Levofloxacin IV Bags Due to Sterility Concerns
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0707-2018·2018-05-09
AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns
AuroMedics Pharma LLC is recalling 67,300 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
Product
LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1609-2018·2018-05-09
Philips MultiDiagnostic-Eleva Imaging System Recalled Due to Uncontrolled Table Rotation
Philips is recalling the MultiDiagnostic-Eleva imaging system because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Product
MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0708-2018·2018-05-09
AuroMedics Recalls Levofloxacin Injection Bags Due to Sterility Concerns
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and reports of leaking bags with mold.
Product
LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1608-2018·2018-05-09
Philips MultiDiagnostic-Eleva Recalled Due to Uncontrolled Table Rotation Hazard
Philips Medical Systems is recalling 184 MultiDiagnostic-Eleva systems because a broken actuator fixation can cause the table to rotate uncontrollably at high speed.
Product
MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1604-2018·2018-05-09
Philips URODiagnost Imaging System Recalled Due to Uncontrolled Table Rotation
Philips Medical Systems is recalling 20 URODiagnost imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Product
708033 URODiagnost As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1476-2018·2018-05-09
FDA Recalls Mitragyna Speciosa Leaf Powder Due to Salmonella Contamination Risk
Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder products because they may be contaminated with Salmonella.
Product
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Exhaust Lines Due to Sterility Concerns
Cook Inc. is recalling 760 StoneBreaker Exhaust Lines because the interior may not be properly sterilized during reprocessing.
Product
StoneBreaker Exhaust Line, Catalog number: SBA-EL; GPN: G52600; UDI: (01)00827002526006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1144-2018·2018-05-09
Purely Elizabeth Granola Recalled for Undeclared Soy Lecithin
Purely Elizabeth is recalling Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin. The product was distributed nationwide.
Product
Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1540-2018·2018-05-09
Siemens Dimension Vista Calcium Flex Reagent Cartridge Recalled for Low Results
Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium Flex reagent cartridges because they may produce erroneously low results from specific well sets.
Product
Dimension Vista¿ Calcium Flex¿ reagent cartridge, Dimension Vista¿ CA, K1023, SMN # 10445160 The CA method is an in vitro diagnostic test for the quantitative measurement of calcium in human serum, plasma, and urine on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2018·2018-05-09
Cook Inc. Recalls StoneBreaker C02 Cartridges Due to Sterility Concerns
Cook Inc. is recalling 38,542 StoneBreaker C02 Cartridges because the interior may not be sterilized to the appropriate level when reprocessed.
Product
StoneBreaker C02 Cartridge, Catalog number: SBC-10; GPN: G52603; UDI: (01)10827002526034
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Probe Caps Due to Sterility Concerns
Cook Inc. is recalling 370 StoneBreaker Probe Caps because the interior may not be properly sterilized during reprocessing.
Product
StoneBreaker Probe Cap, Catalog number:SBA-PC; GPN: G52601; UDI:(01)00827002526013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1591-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Exhaust Caps Due to Sterility Concerns
Cook Inc. is recalling 629 StoneBreaker Exhaust Caps because the interior may not be sterilized to the appropriate level when following reprocessing instructions.
Product
StoneBreaker Exhaust Cap, Catalog number: SBA-EC; GPN: G52599; UDI: (01)00827002525993
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18740·2018-05-09
Wrapables Recalls Women's Silk Scarves for Flammability Standard Violation
Wrapables is recalling about 1,900 women's silk scarves because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Women's scarves
Category
Consumer Product
Distribution
Distributed nationwide