State

Oklahoma product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45926–45950 of 79632

SevereFDA (Drugs)·D-0950-2017·2017-07-12
Phillips Co. Recalls StingMed Insect Bites Skin Protectant Due to GMP Deviations
Phillips Co. is recalling StingMed Insect Bites Skin Protectant because FDA inspections found significant manufacturing deviations that raise questions about the product's safety and quality.
Product
StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume), 0.3 fl. oz. (3 mL) bottle, Phillips Company, Millerton, OK -- NDC 04307-100-11
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2667-2017·2017-07-12
Exactech Equinoxe Reamer Recalled for Updated Instructions on Glenoid Reaming
Exactech is recalling the Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer to update instructions for use, clarifying proper reaming technique to prevent instrument breakage.
Product
EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer Catalog #: 321-45-01
Category
Medical Device
Distribution
33 states
HighFDA (Food)·F-2414-2017·2017-07-12
GoMacro Recalls Specific Thrive Bars Due to Listeria Risk
GoMacro is recalling specific THRIVE Chocolate, Nuts & Sea Salt bars because they may be contaminated with Listeria monocytogenes.
Product
go macro THRIVE Chocolate, Nuts & Sea Salt bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00650 4
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2385-2017·2017-07-12
Bolner's Fiesta Products Recalls Chili Pequino Due to Peanut Contamination
Bolner's Fiesta Products is recalling 26,387 units of Chili Pequino because low levels of peanuts were detected in the product.
Product
Chili Pequino 0.25 oz packaged in a clear plastic bag; Product Code 10106
Category
Food
Distribution
20 states
HighFDA (Food)·F-2413-2017·2017-07-12
GoMacro Recalls Specific MacroBars and Thrive Bars Due to Listeria Risk
GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
Product
go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar, UPC 8 53555-00671 9 and 2. net Wt 2.3 oz / 65 G, UPC 8 53555-00668 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2427-2017·2017-07-12
Ben & Jerry's Chocolate Fudge Brownie Pint Slices Recalled for Undeclared Peanut
Unilever is voluntarily recalling Ben & Jerry's Chocolate Fudge Brownie Pint Slices due to undeclared peanut.
Product
Ben & Jerry's Pint Slices Chocolate Fudge Brownie 3 chocolate ice cream bars Net 9 FL OZ. UPC code 076840657940
Category
Food
Distribution
Distributed nationwide
HighCPSC·17185·2017-07-12
TriggerTech Recalls Crossbow and Rifle Triggers Due to Injury Hazard
TriggerTech is recalling about 2,000 carbide crossbow and rifle triggers because rollers can crack, causing the weapon to discharge without trigger activation.
Product
TriggerTech Carbide crossbow and rifle triggers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-2415-2017·2017-07-12
GoMacro Recalls Thrive Caramel Coconut Bars for Listeria Risk
GoMacro is recalling specific THRIVE Caramel Coconut bars because they may be contaminated with Listeria monocytogenes.
Product
go macro THRIVE Caramel Coconut bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00652 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2685-2017·2017-07-12
PerkinElmer Multiphor II Electrophoresis System Recalled for Electric Shock Risk
PerkinElmer is recalling 241 Multiphor II Electrophoresis Systems due to a potential electric shock hazard if grommets are not installed.
Product
Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2672-2017·2017-07-12
Ion Beam Applications Recalls Proteus Proton Therapy Systems for Software Issues
Ion Beam Applications is recalling Proteus 235 and Proteus ONE proton therapy systems because on-site software installations were not performed consistently with standard operating procedures.
Product
Proteus 235 and Proteus ONE proton therapy systems
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-2658-2017·2017-07-12
Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-packaging Error
Encore Medical is recalling 9 units of 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.
Product
3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2665-2017·2017-07-12
Exactech Equinoxe Modular Reverse Pilot-Tip Starter Reamer Recall
Exactech is recalling 928 Equinoxe Modular Reverse Pilot-Tip Starter Reamers to update instructions for use. The update clarifies proper reaming technique to prevent instrument breakage.
Product
EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #: 321-25-01
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2664-2017·2017-07-12
Exactech Equinoxe Glenoid Reamer Recalled for Updated Instructions
Exactech is recalling Equinoxe Glenoid Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38, Catalog #: 321-05-42, and Catalog #: 321-05-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2668-2017·2017-07-12
Exactech Equinoxe Reamer Recall Due to Updated Instructions for Use
Exactech is recalling Equinoxe Narrow Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #: 321-45-38, Catalog #: 321-45-42 and Catalog #: 321-45-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2663-2017·2017-07-12
Exactech Equinoxe Reverse Starter Reamer Recalled for Updated Instructions
Exactech is recalling 382 Equinoxe Reverse Starter Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2662-2017·2017-07-12
Exactech Recalls Logic Fit Tibial Tamp Heads for Labeling Clarification
Exactech, Inc. is recalling 573 Logic Fit Tibial Tamp Heads to update surgical labeling. The update clarifies proper removal techniques to prevent instrument breakage.
Product
Logic Fit Tibial Tamp Head
Category
Medical Device
Distribution
32 states
ModerateFDA (Drugs)·D-0945-2017·2017-07-12
G & W Clobetasol Propionate Ointment Recalled for Impurity
G & W Laboratories is recalling Clobetasol Propionate Ointment 0.05% due to out-of-specification results for a known impurity.
Product
CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0937-2017·2017-07-12
Methocarbamol USP Recalled for Quality Assurance Deviations
American Pharmaceutical Ingredients LLC is recalling Methocarbamol USP due to lack of quality assurance at the API manufacturer.
Product
Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2666-2017·2017-07-12
Exactech Equinoxe Modular Reverse Pilot-Tip Reamer Recall for Labeling Clarification
Exactech is recalling Equinoxe Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2645-2017·2017-07-12
Boston Scientific Imager II Angiographic Catheter Recall for Missing Seal
Boston Scientific is recalling Imager II Angiographic Catheters because some units are missing the bottom pouch seal. The defect is obvious to the user.
Product
Boston Scientific Imager II Angiographic Catheter, a pathway for delivering contrast media to selected sites in the vascular system. M001314141 (5-pack outer package UPN), M001314140, single unit, inner package UPN)
Category
Medical Device
Distribution
9 states
ModerateFDA (Drugs)·D-0944-2017·2017-07-12
GSK Recalls Parodontax Toothpaste Due to Possible Metal Presence
GSK Consumer Healthcare is recalling 15,708 tubes of Parodontax Whitening toothpaste due to the possibility of metal in the product.
Product
PARODONTAX — PARODONTAX (STANNOUS FLUORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0934-2017·2017-07-12
PharMEDium Recalls Ropivacaine HCl Injection Due to Labeling Errors
PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0935-2017·2017-07-12
PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.
Product
Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2659-2017·2017-07-12
Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging
Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.
Product
3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0932-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors
PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
Category
Drug
Distribution
Distributed nationwide