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.

42476–42500 of 79629

HighFDA (Devices)·Z-0982-2018·2018-03-21
Alden Optical Recalls NovaKone Toric Contact Lenses for Sterility Issues
Alden Optical is recalling 33 units of NovaKone Toric Daily Wear Soft contact lenses because they lack sterility assurance. The lenses were distributed in 25 US states and Canada.
Product
NovaKone Toric Daily Wear Soft contact; Catalog Number: AONKT54 Product Usage: The NOVAKONE TORIC lens is indicated for daily wear for persons requiring keratoconus management for the correction of refractive ametropia (myopia, hyperopia and astigmatism) in aphakic and not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1072-2018·2018-03-21
Zimmer Biomet Recalls TunneLoc Tibial Fixation Devices Due to Sterilization Concerns
Zimmer Biomet is recalling TunneLoc Tibial Fixation Devices because testing suggests the sterilization dose may be inadequate. The devices are distributed nationwide.
Product
TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: To provide fixation of soft tissue grafts within the tibial tunnel during anterior cruciate ligament (ACL) and/or posterior cruciate ligament (PCL) reconstruction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0934-2018·2018-03-21
Ion Beam Applications Recalls Proteus 235 Proton Therapy Systems
Ion Beam Applications is recalling 14 Proteus 235 proton therapy systems because an accessory can be improperly inserted, allowing the device to operate incorrectly.
Product
Proteus 235, Uniform and Pencil Beam Scanning The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions…
Category
Medical Device
Distribution
6 states
HighNHTSA·18E016000·2018-03-21
BMW Recalls Accessory Motorcycle Windscreens Due to Visibility Issues
BMW is recalling specific accessory windscreens for various motorcycle models because extra tinting may reduce rider visibility, increasing crash risk.
Product
BMW — BMW R1200 R, S1000 R, S1000 XR, F700 GS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0986-2018·2018-03-21
Alden Optical Recalls HP59 Sphere Daily Wear Soft Contact Lenses
Alden Optical is recalling HP59 Sphere Daily Wear Soft contact lenses because they lack sterility assurance. The recall affects units distributed in the US and Canada.
Product
Alden HP59 Sphere Daily Wear Soft contact; Catalog Number: AOHPS59 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia).…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0925-2018·2018-03-21
Plant Divas Lemongrass Facial Polish Recalled for Microbial Contamination
Plant Divas Inc. is recalling Lemongrass Facial Polish with Oats, Fengreek & Neem because FDA testing found excessive numbers of microorganisms.
Product
Lemongrass Facial Polish with Oats, Fengreek & Neem. 3 oz cylindrical box evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1065-2018·2018-03-21
Siemens ACUSON SC2000 Ultrasound System Recalled for EROA Underestimation
Siemens Medical Solutions is recalling 564 ACUSON SC2000 ultrasound systems because a specific application may underestimate the Effective Regurgitant Orifice Area (EROA) compared to other transducers.
Product
ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult Cephalic, Peripheral Vessel, Abdominal, Abdominal Intraoperative…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1028-2018·2018-03-21
Zimmer Biomet Recalls Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling specific Versys hip prostheses because LDPE packaging may leave residue on the polished implant surface.
Product
VERSYS 7.5 INCH BEADED FC REV 13.5X190MM STRAIGHT Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1014-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
BIPOLAR METAL SHELL 48 MM OD Use of the MultiPolar Bipolar Cup is indicated in: Total hip replacement
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0980-2018·2018-03-21
Zimmer Biomet Recalls Humeral Stems Due to Incorrect Lot Number Etching
Zimmer Biomet is recalling 12 Humeral Stems because two lots were commingled and etched with incorrect lot numbers, creating a risk of using the wrong implant size.
Product
Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and revision total shoulder arthroplasty as well as hemi-arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18128·2018-03-21
Kidde Recalls Dual-Sensor Smoke Alarms Due to Manufacturing Defect
Kidde is recalling about 452,000 dual-sensor smoke alarms in the U.S. because a manufacturing defect may prevent them from detecting smoke.
Product
Kidde dual-sensor (photoelectric and ionization) smoke alarms - models PI2010 and PI9010
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0917-2018·2018-03-21
Kodiak Cakes Energy Waffles Recalled for Undeclared Milk Allergen
Kodiak Cakes is recalling Energy Waffles, Blueberry Chia, because the product contains whey but fails to declare the major food allergen milk on the label.
Product
Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 Oz (304 g), Kodiak Cakes, Park City, UT. Packaging configuration: 8-ct chipboard carton (selling unit); 8 cartons per shipping case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0988-2018·2018-03-21
Alden HP54 Toric Contact Lenses Recalled for Sterility Assurance Issues
Alden Optical is recalling HP54 Toric Daily Wear Soft contact lenses because they lack sterility assurance. Consumers should stop using the affected lenses.
Product
Alden HP54 Toric Daily Wear Soft contact; Catalog Number: AOHPT54 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0928-2018·2018-03-21
Plant Devas Rose Face Care Kit Recalled for Microbial Contamination
Plant Devas Inc. is recalling Rose Face Care Kits because FDA testing found excessive and virulent microorganisms in the products.
Product
Rose Face Care Kit; Each kit contains: Rose Cleansing Milk -- 1 fl oz bottle Rose Geranium Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - ROSE 0.13 fl oz vial Rose Vetiver Day Moisturizer 0.17 fl oz jar French Rose Clay 0.1 oz jar…
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1017-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling specific hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
CPT 12/14 COCR SIZE 1 EXT prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0987-2018·2018-03-21
Alden HP49 Toric Contact Lenses Recalled for Sterility Assurance Issues
Alden Optical is recalling 56 units of Alden HP49 Toric Daily Wear Soft contact lenses because they lack sterility assurance. The lenses were distributed in 25 US states and Canada.
Product
Alden HP49 Toric Daily Wear Soft contact; Catalog Number: AOHPT49 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1074-2018·2018-03-21
Smiths Medical Recalls Misassembled Power PORT-A-CATH II Implantable Port Kits
Smiths Medical ASD Inc. is recalling 1,077 units of Power PORT-A-CATH II kits that may contain incorrect introducer sizes or locking collars.
Product
Power PORT-A-CATH II, TRAY POWER PAC II. Labeled as: a. VEN, PU, 2.6MM, UL 8.5 FR/INTRO, VALVED (1/EA); b. VEN LP, PU, 2.6MM, UL 8.5 FR/INTRO, VALVED (1/EA); c. VEN LP, PU, 1.9MM, UL, 6 FR/INTRO, VALVED (1/EA); d. DL, LP, PU, 2.2MM, WING-LOCK, 7FR, INTRO (1/EA)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1025-2018·2018-03-21
Zimmer Biomet Recalls Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling specific Versus hip prostheses because LDPE packaging may leave residue on the polished implant surface.
Product
VERSYS 6 INCH BEADED FC 15X160MM STD BODY STD NECK Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1070-2018·2018-03-21
Stanbio Recalls RaPET RF Latex Reagent Due to False Positive Test Results
Stanbio Laboratory is recalling RaPET RF Latex Reagent because it causes all patient serum samples to yield weakly positive test results.
Product
RaPET¿ RF Latex Reagent used as a component in the following kits: RaPET RF (1155-100, Control# 173201 expiry 2019-04-30) RF Latex (1156-001, Control# 172224 expiry 2019-12-31) RF Latex (1155L-100B, Control # 172701 expiry 2019-09-30 and Control # 173262 expiry 2019-12-31)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0929-2018·2018-03-21
Plant Devas Blue Face Care Kit Recalled for Microbial Contamination
Plant Devas Inc. is recalling the Blue Face Care Kit because FDA testing found excessive and virulent microorganisms in the product.
Product
Blue Face Care Kit; Each kit contains: Blue Lavender Cleansing Milk 1 fl oz bottle Lavender Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - BLUE 0.13 fl oz vial Blue Chamomile Day Moisturizer 0.17 fl oz jar Green Tea Clay 0.1 oz jar…
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0977-2018·2018-03-21
ZOLL Adult Defibrillator Electrodes Recall for Pediatric Energy Delivery Risk
ZOLL Medical is recalling specific adult defibrillator electrodes that may cause R Series devices to deliver pediatric energy levels instead of adult levels.
Product
OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI: 10847946016279) and 8900 0224 01 (single electrode, UDI: 00847946016272) Product Usage: Intended Use: Defibrillation, Cardioversion, Noninvasive Pacing, EGG…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2018·2018-03-21
Alden Classic 55 Toric Contact Lenses Recalled for Sterility Issues
Alden Optical is recalling Alden Classic 55 Toric Daily Wear Soft contact lenses because they lack sterility assurance. The recall affects units distributed in the US and Canada.
Product
Alden Classic 55 Toric Daily Wear Soft contact; Catalog Number: AOCLT55 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0968-2018·2018-03-21
BD Vacutainer K2 EDTA Blood Collection Tubes Recalled for Additive Deficiency
Becton Dickinson is recalling specific lots of BD Vacutainer K2 EDTA blood collection tubes because they may contain insufficient anticoagulant, potentially causing erroneous test results.
Product
BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole blood hematology determinations, immunohematology testing and blood donor screening.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1037-2018·2018-03-21
Zimmer Biomet Recalls Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 knee implants because LDPE packaging may leave residue on the polished surface.
Product
LCCK FEM IMPLANT SZ C-L LCCK FEM IMPLANT SZ C-R LCCK FEM IMPLANT SZ D-R LCCK FEM IMPLANT SZ E-L LCCK FEM IMPLANT SZ E-R LCCK FEM IMPLANT SZ F-L LCCK FEM IMPLANT SZ F-R This device is indicated for patients with severe knee pain and disability
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1029-2018·2018-03-21
Zimmer Biomet Recalls Versus 8 Inch Beaded Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 Versus 8 Inch Beaded hip implants because LDPE packaging may leave residue on the polished surface.
Product
VERSYS 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM STR STD BODY/NECK 14X200MM STR STD BODY/NECK REV 13.5X200MM BWD LT 15X200MM STR STD BODY/NECK REV 13.5X200MM BWD RT REV 15.0X200MM BWD LT REV 15.0X200MM BWD RT REV 16.5X200MM BWD LT REV 16.5X200MM BWD RT…
Category
Medical Device
Distribution
Distributed nationwide