State

Oklahoma product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31601–31625 of 79544

HighFDA (Devices)·Z-1564-2020·2020-04-01
Capintec Captus 4000e Thyroid Uptake System Recall for Collimator Defect
Capintec is recalling Captus 4000e Thyroid Uptake Systems because insufficiently tapped screw holes may allow the collimator assembly to fall and contact patients or operators.
Product
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1558-2020·2020-04-01
Abbott FreeStyle Precision H Blood Glucose and Ketone Meter Recall
Abbott is recalling FreeStyle Precision H meters because unapproved instructions for disinfection and multi-patient use may lead to infection.
Product
FreeStyle Precision H Blood Glucose and Ketone Monitoring System, UDI: 00093815711810
Category
Medical Device
Distribution
32 states
ModerateFDA (Food)·F-0904-2020·2020-04-01
Pure Planet Organic Parasite Cleanse Recalled for Unapproved Herbicide
Organic By Nature, Inc. is recalling Pure Planet Organic Parasite Cleanse because the flaxseed powder ingredient contains the unapproved herbicide Haloxyfop.
Product
Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Jar; Finished Product Item # 52700 Manufactured and Distributed by: Pure Planet, Rancho Dominguez, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1574-2020·2020-04-01
Bard Groshong Dual-Lumen Catheters Recalled for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 650 Groshong 9.5 Dual-Lumen CV Catheters because they may contain an incorrect tunneler barb tip, potentially prolonging surgical operations.
Product
1. Groshong 9.5 Dual-Lumen CV Catheter, Ref: 7726950, UDI: (01)00801741041570; 2. Groshong 9.5 F Dual-Lumen CV Catheter, REF: 7726954, UDI: (01)00801741041587
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0906-2020·2020-04-01
Organic Super Protein Vanilla Coconut Recalled for Unapproved Herbicide
Organic By Nature, Inc. is recalling Touchstone Essentials Organic Super Protein Vanilla Coconut due to unapproved herbicide Haloxyfop in the flaxseed ingredient.
Product
Touchstone Essentials Organic Super Protein Vanilla Coconut; Whole Food Dietary Supplement; Net Wt. 18.3 oz. (520g) Plastic Bottle; Finished Product Item#: FTEVPVC520G Manufactured Exclusively for: Touchstone Essentials, Raleigh, NC
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0903-2020·2020-04-01
Springboard Green Power Recalled for Unapproved Herbicide Contamination
Organic By Nature, Inc. is recalling Springboard Green Power dietary supplements because the flaxseed ingredient contains an unapproved herbicide.
Product
Springboard Green Power, Dietary Supplement; 240g Plastic Bottle; Finished Product Item# FSBPGO240G Springboard, Spring Valley, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1576-2020·2020-04-01
BardPort M.R.I. Implantable Port Recall Due to Incorrect Catheter Tip
Bard Peripheral Vascular Inc is recalling BardPort M.R.I. Implantable Ports because they may contain an incorrect catheter tip, potentially prolonging surgical operations.
Product
BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended Single-Lumen Venous Catheter, REF: 0602680, UDI:(01)00801741025679 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1538-2020·2020-04-01
Siemens ADVIA Chemistry Direct Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Direct Bilirubin assays because they may show positive bias in patients taking eltrombopag.
Product
ADVIA Chemistry Direct Bilirubin_2 assay-SMN: 10316610 (20 mL) & 10341114 (70 mL) - Product Usage: ADVIA DBIL_ 2 is for in vitro diagnostic use in the quantitative determination of direct bilirubin in human serum and plasma on the ADVIA¿ Chemistry systems. Such measurements are…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1575-2020·2020-04-01
BardPort Titanium Implantable Port Recall Due to Incorrect Catheter Tip
Bard Peripheral Vascular Inc is recalling 360 BardPort Titanium Implantable Ports because they may contain an incorrect catheter tip, potentially prolonging surgery.
Product
BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter , REF: 0602230, UDI: (01)00801741025563 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port system…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1579-2020·2020-04-01
Bard PowerFlow Apheresis IV Port Recalled for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 296 PowerFlow Implatable Apheresis IV Ports because they may contain an incorrect tunneler tip, potentially prolonging surgical operations.
Product
PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl x Open-Ended Single-Lumen Venous Catheter, Ref A710962, UDI:(01)00801741129438 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1537-2020·2020-04-01
Siemens Atellica CH Total Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling Atellica CH Total Bilirubin assays because they may show inaccurate high results for patients taking eltrombopag.
Product
Atellica CH Total Bilirubin_2 assay-In vitro Diagnostic for the determination of total bilirubin SMN: 11097531 - Product Usage: Atellica TBil_2 assay is for in vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma (lithium heparin)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1540-2020·2020-04-01
Siemens Total Bilirubin Reagent Cartridge Recall for Eltrombopag Interference
Siemens Healthcare is recalling Dimension Total Bilirubin Flex reagent cartridges because the assay may show falsely high results for patients taking eltrombopag.
Product
Dimension Total Bilirubin Flex reagent cartridge -In vitro Diagnostic for the determination of total bilirubin. SMN: 10444957 Product Usage: Dimension TBI method for the ¿ clinical chemistry syst6em is an in vitro diagnostic test intended to quantitatively measure total…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0900-2020·2020-04-01
Organic By Nature Recalls L.O.V.E. Supermeal Original Due to Unapproved Herbicide
Organic By Nature, Inc. is recalling L.O.V.E. Supermeal Original products because the organic ground flaxseed powder ingredient was found to contain the unapproved herbicide Haloxyfop.
Product
L.O.V.E. Supermeal Original: 420g Plastic Bottle, 1396g Plastic Bottle, 693g Bio Bag Terra Pouch; Finished Product Item # 2700E, 2711, 2712, 2712-P65 Platinum Health Europe, Netherlands, Purim Health Products, Rancho Dominguez, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1544-2020·2020-04-01
Medline Stick Sponge Presaturated W/PVP Recalled for Packaging Seal Voids
Medline is recalling Stick Sponge Presaturated W/PVP units due to packaging seal voids that compromise sterility.
Product
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1536-2020·2020-04-01
Siemens Atellica CH Direct Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling Atellica CH Direct Bilirubin assays because they may show inaccurate results for patients taking eltrombopag.
Product
Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the determination of direct bilirubin SMN: 11097532 - Product Usage: ADVIA DBIL_ 2 is for in vitro diagnostic use in the quantitative determination of direct bilirubin in human serum and plasma on the ADVIA¿ Chemistry…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1573-2020·2020-04-01
Bard Vaccess CT Implantable Port Recall Due to Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 598 Vaccess CT Power-Injectable Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Product
1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs, Ref: 7496000, UDI:(01)00801741027482 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0905-2020·2020-04-01
Touchstone Essentials Super Greens Juice Recalled for Unapproved Herbicide
Organic By Nature, Inc. is recalling Touchstone Essentials Super Greens Juice due to the presence of the unapproved herbicide Haloxyfop in an ingredient.
Product
Touchstone Essentials Super Greens Juice - Raspberry Apple; Premium Organic Superfood Juice Powder: Whole Food Dietary Supplement; Net Wt. 10.5 oz. (300 g) Plastic Bottle; Finished Product Item#: FTSGJRA300G Manufactured Exclusively for: Touchstone Essentials, Raleigh…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1571-2020·2020-04-01
Bard PowerPort M.R.I. Implantable Port Catheter Recall for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 878 PowerPort M.R.I. Implantable Port catheters because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Product
1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1809600, UDI: (01)00801741027130 ; 2. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter Without Suture…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0898-2020·2020-04-01
Organic By Nature Daily Fiber Blend Recalled for Unapproved Herbicide
Organic By Nature is recalling Daily Fiber Blend - Caramel Apple Flavor because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.
Product
Daily Fiber Blend - Caramel Apple Flavor; Organic Plant Powder Mix for preparation of a fiber-rich drink, 540g Plastic Bottle, 180g Bio Bag Terra Pouch; Finished Product Item#: 2012E, 2012, 2012-P65, 2013, 2013-P65, 2016, 2016-P65 Brand names of: Platinum Health Europe…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1577-2020·2020-04-01
BardPort M.R.I. Hard Base Implantable Port Recall Due to Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 151 BardPort M.R.I. Hard Base Implantable Ports because they may contain an incorrect tunneler barb tip, potentially prolonging surgical operations.
Product
BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter, Ref: 0604550, UDI: (01)00801741025860 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0895-2020·2020-04-01
Organic By Nature Chia/Flax Boost Recalled for Unapproved Herbicide
Organic By Nature is recalling Chia/Flax Boost dietary supplements because the flaxseed powder contains unapproved herbicide Haloxyfop.
Product
care/of Chia/Flax Boost Dietary Supplement; Net Wt. 0.35 oz. (10g) foil packets; Finished Product Item # FCOFBP10G Distributed by Noho Health Inc., New York, NY 10013
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1529-2020·2020-04-01
Fresenius Medical Care Recalls Honeywell Pressure Transducers for Hemodialysis Systems
Fresenius Medical Care is recalling 3,561 Honeywell pressure transducers used in hemodialysis delivery systems due to lower long-term reliability.
Product
Honeywell Pressure Transducer- Part Number: 370506-22. It is a component used in 2008T, Common Name: Hemodialysis Delivery System; 2008T HD SYS. BLUE STAR; 2008K2, Common Name: Hemodialysis Delivery Equipment; 2008K@home, Common Name: Hemodialysis Delivery System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0901-2020·2020-04-01
Organic By Nature Supermeal Vanilla Chai Recalled for Unapproved Herbicide
Organic By Nature is recalling L.O.V.E. Supermeal Vanilla Chai because it contains Organic Ground Flaxseed powder contaminated with the unapproved herbicide Haloxyfop.
Product
L.O.V.E. Supermeal Vanilla Chai: 1320g Plastic Bottle, 660g Bio Bag Terra Pouch; Finished Product Item #: 2910E, 2910, 2910-P65, 2911, 2911-P65 Platinum Health Europe, Netherlands, Purim Health Products, Rancho Dominguez, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1539-2020·2020-04-01
Siemens ADVIA Chemistry Total Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Total Bilirubin assays because they may show falsely high results for patients taking eltrombopag.
Product
ADVIA Chemistry Total Bilirubin_2 assay- SMN: 10341115 (40 mL) & 10341113 (70 mL). Product Usage: ADVIA TBIL_2 is for in vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma of adults and neonates on the ADVIA¿ Chemistry…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1578-2020·2020-04-01
Bard X-Port isp MRI Implantable Port Recall for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 225 X-Port isp MRI Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Product
1. X-Port isp M.R.I Implantable Port, with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter, REF:0607550, UDI:(01)00801741026195 2. X-Port isp M.R.I. Implantable Port, with Attachable 9.6F Open-Ended Single-Lumen Venous Catheter, REF: 0657525, UDI:(01)00801741026379…
Category
Medical Device
Distribution
Distributed nationwide