State

Oklahoma product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34901–34925 of 79559

HighFDA (Devices)·Z-2240-2019·2019-08-21
BioPro K-Wire Sterile Single Trochar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling K-Wire Sterile Single Trochar units due to a manufacturing flaw in the sterile barrier system that may compromise sterility.
Product
K-Wire Sterile Single Trochar, Item Number 19106 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2230-2019·2019-08-21
Elekta iGUIDE System Recalled for Potential Position Monitoring Error
Elekta is recalling 374 iGUIDE Systems because they may incorrectly monitor 3D position. The recall covers devices distributed nationwide and worldwide.
Product
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2253-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x115 due to a manufacturing flaw in the sterile barrier system. The devices are intended for orthopedic surgical procedures.
Product
Go-EZ Screw 6.5x115, Item Number 19671 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2242-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 350 units of K-Wire Single Trocar 2.5x170mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 2.5x170mm, Item Number OL17025S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2259-2019·2019-08-21
BioPro K-Wire HBS Sterile Lots Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 17 units of K-Wire HBS Sterile Lots due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire HBS Sterile Lot, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2246-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x30 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x30, Item Number 19651 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2271-2019·2019-08-21
Siemens SOMATOM Drive CT Systems Recalled for Software Safety Issues
Siemens Medical Solutions is recalling SOMATOM Drive CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Drive, Model Number 10431700 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2055-2019·2019-08-21
Amy's Kitchen Recalls Broccoli and Cheddar Bake Due to Foreign Material
Amy's Kitchen Inc. is recalling 5,207 cases of Broccoli & Cheddar Bake due to consumer complaints of black plastic found in the product.
Product
Amy's Bowls - Broccoli & Cheddar Bake; Net Wt. 9.5 oz. (269g) Perishable - Keep Frozen. Microwave or regular oven. UPC: 0 42272 00811 7 Amy's kitchen Inc., P.O. Box 7129, Petaluma, CA 94955 INGREDIENTS: RICE PASTA (ORGANIC RICE FLOUR, FILTERED WATER, ORGANIC POTATO…
Category
Food
Distribution
27 states
HighNHTSA·19V612000·2019-08-21
Rolls-Royce Cullinan Recall for Dim Brake Lights
BMW is recalling 2019 Rolls-Royce Cullinan vehicles because brake lights may not be bright enough, increasing crash risk.
Product
ROLLS-ROYCE — ROLLS-ROYCE CULLINAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2270-2019·2019-08-21
Siemens SOMATOM CT Systems Recalled for Software Scan Abort Risk
Siemens is recalling SOMATOM Definition Flash CT systems due to four software issues that may cause scans to abort.
Product
SOMATOM Definition Flash, Model Number 10430603 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2248-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x36 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x36, Item Number 19654 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2268-2019·2019-08-21
Siemens SOMATOM Definition AS CT Systems Recalled for Software Issues
Siemens Medical Solutions USA is recalling SOMATOM Definition AS CT systems due to four safety-related software issues in syngo.CT version VB10A that may cause scan aborts.
Product
SOMATOM Definition AS, Model Number 8098027 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2256-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x110 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x110, Item Number 19670 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2244-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 350 units of K-Wire Single Trocar 1.1x150mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 1.1x150mm, Item Number OL15011S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2250-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x34 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x34, Item Number 19653 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2243-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 350 units of K-Wire Single Trocar 1.6x150mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 1.6x150mm, Item Number OL15016S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2241-2019·2019-08-21
BioPro K-Wire Sterile Single Trochar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling K-Wire Sterile Single Trochar units due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Sterile Single Trochar .045, Item Number 19108 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2233-2019·2019-08-21
Zimmer Biomet Recalls Orthopedic Salvage System Hybrid Poly Tibia Components
Zimmer Biomet is recalling 23 Orthopedic Salvage System Hybrid Poly Tibia units because cleaning processes may be ineffective. The products were distributed to 18 US states, Japan, and the Netherlands.
Product
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2252-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x90 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x90, Item Number 19666 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2273-2019·2019-08-21
Siemens SOMATOM Edge Plus CT Systems Recalled for Software Issues
Siemens is recalling SOMATOM Edge Plus CT systems due to four safety-related software issues in syngo.CT version VB10A that may cause scan aborts.
Product
SOMATOM Edge Plus, Model Number 10267000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2019·2019-08-21
Zimmer Biomet Recalls Orthopedic Salvage System Hybrid Poly Tibia Components
Zimmer Biomet is recalling 28 Orthopedic Salvage System Hybrid Poly Tibia units because cleaning processes may be ineffective. The products were distributed in the US and internationally.
Product
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811
Category
Medical Device
Distribution
18 states
HighFDA (Food)·F-2019-2019·2019-08-21
Kerry Predust Batter Recalled for Nylon String Foreign Material
Kerry, Inc. is recalling 104 bags of Predust/Batter due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine states.
Product
Predust/Batter, Item Number 30753195.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-2257-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x120 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x120, Item Number 19672 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2053-2019·2019-08-21
Kerry Breader Recalled Due to Nylon String Foreign Material
Kerry, Inc. is recalling 258 bags of Breader because the product contains nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Product
Breader, Item Number 30753230.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-2247-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x100 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x100, Item Number 19668 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide