State

Oklahoma product recalls

72,820 recalls have nationwide distribution and so reach Oklahoma. 5,785 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,785
Critical: 1,031
Severe: 1,237
Most recent: 2026-09-02

Of the 5,785 recalls naming Oklahoma we have scored against our rubric, 1,031 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,237 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,785 recalls whose distribution notice names Oklahoma specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

651–675 of 78605

SevereFDA (Devices)·Z-2688-2026·2026-07-22
Abiomed Impella 5.5 SmartAssist S2 heart pump introducer sheath leakage risk
Abiomed is recalling Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines that may not be visible to users.
Product
ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2708-2026·2026-07-22
Arterial Line Kit with Lidocaine HCL Injection Fails Sterility Testing
Argon Medical Devices is recalling an Arterial Line Kit containing Lidocaine HCL Injection USP because the kits do not meet sterility release criteria, creating a risk of infection from non-sterile medical injection.
Product
Arterial Line Kit 20ga x 6, REF: 400115A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0690-2026·2026-07-22
ChloraPrep One-Step Applicators Recalled for Potential Packaging Seal Defects
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) applicators nationwide because affected units may have open or incomplete seals on the packaging, which could compromise sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2739-2026·2026-07-22
Medtronic Bio-Medicus Adult Cannula Kit Recalled for Foreign Material
Medtronic is recalling its Bio-Medicus Adult Cannula Kit (Product Number 96530-115) used in cardiopulmonary bypass procedures due to the discovery of loose foreign material containing trace levels of blood in two units.
Product
Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1154-2026·2026-07-22
Pillsbury Bread Rolls Hard Roll Dough Recalled for Glass
General Mills is recalling Pillsbury Bread Rolls Hard Roll Dough due to potential glass contamination. Affected products were distributed across multiple states.
Product
Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-2726-2026·2026-07-22
GE Medical Optima XR200/220/240amx Mobile Radiographic Systems Recall
GE HealthCare recalls certain Optima XR200/220/240amx mobile radiographic systems where safety testing may have been incomplete after column replacement. A failed counterpoise cable could cause the X-ray arm to drop on patients.
Product
Optima XR200amx, Mobile Digital-Ready Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2728-2026·2026-07-22
Mobile Digital Radiographic System Arm Drop Risk During Patient Exams
GE HealthCare is recalling certain Optima XR200/220/240amx Mobile Digital Radiographic Systems due to potential failure of the Column Safety mechanism, which could cause the X-ray arm to drop during patient exams. The issue stems from incomplete functional testing of the safety pawl after column replacement.
Product
Optima XR240amx, Mobile Digital Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1155-2026·2026-07-22
Pillsbury Kaiser Roll Dough recalled for potential glass contamination
General Mills is recalling Pillsbury Bread Rolls, Kaiser Roll Dough due to potential foreign glass material in the product. Affected consumers should not consume the product and should contact the company or retailer for a refund.
Product
Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz each. Net Wt. 22.5 lb (10.2kg) Package UPC 7 21582-13288 9. Case UPC 107-21582-13288-6. Keep Frozen. Case Qty 144. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-2718-2026·2026-07-22
Olympus Toomey Evacuator 30cc medical device sterilization parameters recalled
Olympus Corporation recalled the Toomey Evacuator 30cc with Adaptor (Model 188) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
Product
Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2738-2026·2026-07-22
Medtronic DLP One-Piece Pediatric Arterial Cannula Recalled for Foreign Material
Medtronic is recalling certain DLP One-Piece Pediatric Arterial Cannulas (Product Number 77010) due to complaints of loose foreign material containing trace levels of blood found in the devices.
Product
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2719-2026·2026-07-22
Olympus Toomey Evacuator 50cc with Adaptor sterilization recall
Olympus is recalling the Toomey Evacuator 50cc with Adaptor (Model 188A) because some sterilization parameters in the instructions may not reliably render the devices sterile.
Product
Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V471000·2026-07-22
ATC Recalls 2026 RM500 and RM700 Trailers Due to Winch Remote Issue
Aluminum Trailer Company is recalling 2026 RM500 and RM700 trailers because the wireless remote may cause unexpected winch movements, increasing injury risk.
Product
ATC — ATC RM500, RM700
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V473000·2026-07-22
2024–2026 Volkswagen Atlas and Atlas Cross Sport Rearview Camera Software
Volkswagen is recalling 2024–2026 Atlas and Atlas Cross Sport vehicles due to a low-voltage electrical event that may cause the rearview camera display to fail, reducing rear visibility.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V475000·2026-07-22
Freightliner Trucks Recalled for Low Beam Headlight Software Error
Daimler Trucks North America is recalling 2026-2027 Freightliner models because a software error may cause low beam headlights to illuminate improperly, increasing crash risk.
Product
FCCC — FCCC, FREIGHTLINER S2C, S2RV, BUSINESS CLASS M2, EM2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V472000·2026-07-22
Coach and Equipment Recalls Phoenix and Metrolite Buses with Lift Defect
Coach and Equipment is recalling 2024-2026 Phoenix and Metrolite buses because a wheelchair lift may fail to stop, increasing injury risk.
Product
COACH AND EQUIPMENT — COACH AND EQUIPMENT METROLITE, PHOENIX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2725-2026·2026-07-22
Rapid Refill Continuous Injection System Recalled for Syringe Loosening Risk
Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.
Product
Rapid Refill Continuous Injection System, UPN M00566001
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26E047000·2026-07-22
Hiab Recalls K-HiPro Cranes Due to Potential Column Weld Failure
Hiab USA Inc. is recalling K-HiPro 425 and 505 cranes because a weld may crack, risking column collapse and injury.
Product
EQUIPMENT:MECHANICAL:BOOM/CRANE/LADDER recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2727-2026·2026-07-22
GE Optima XR200/220/240amx Radiographic System Column Safety Mechanism
GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.
Product
Optima XR220amx, Mobile Digital-Ready Radiographic System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2721-2026·2026-07-22
Olympus Glass Body for 194 Ellik Evacuator Model 190A Sterilization Recall
Olympus Corporation is recalling the Glass Body for 194 Ellik Evacuator (Model 190A) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.
Product
Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2741-2026·2026-07-22
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
Maquet Cardiovascular is recalling Vasoview Hemopro 2 devices from Lot 3000547797 due to exposure to out-of-specification sterilization during gamma sterilization. The affected devices may not be properly sterilized.
Product
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2744-2026·2026-07-22
Photera 600 3-D phototherapy device UV sensor calibration error recall
Daavlin Distributing Company is recalling Photera 600 3-D phototherapy devices because the UV sensor gain calculation is incorrect, causing inaccurate ultraviolet output measurement.
Product
Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2742-2026·2026-07-22
Photera 400 Phototherapy Device Recalled for Incorrect UV Sensor Calibration
Daavlin Distributing Company is recalling the Photera 400 phototherapy device because the UV sensor calibration is calculating incorrectly, resulting in lower output levels than intended.
Product
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0686-2026·2026-07-22
Foster & Thrive Carbamide Peroxide 6.5% Recalled for Subpotent Strength
Bell Pharmaceuticals recalls Foster & Thrive Carbamide Peroxide 6.5% due to subpotent drug substance with low pH and significantly reduced assay levels. Approximately 31,094 units distributed nationwide are affected.
Product
Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0682-2026·2026-07-22
Audiologist's Choice Carbamide Peroxide Earwax Removal Recalls
Bell Pharmaceuticals is recalling Audiologist's Choice Carbamide Peroxide earwax removal product due to subpotency: the active ingredient concentration is approximately 0.6% instead of the expected 6–7%, and the product has low pH.
Product
AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM — AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0688-2026·2026-07-22
CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient
CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.
Product
CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE)
Category
Drug
Distribution
Distributed nationwide