State

Oklahoma product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50451–50475 of 79640

ModerateFDA (Devices)·Z-2859-2016·2016-09-28
Abbott Recalls Intraocular Lenses Due to Mislabeled Product Release
Abbott Medical Optics is recalling 131 TECNIS OptiBlue intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS OptiBlue 1-Piece Intraocular Lens (IOL), Model No. ZCB00V The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2857-2016·2016-09-28
Abbott Recalls TECNIS Symfony Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 10 TECNIS Symfony intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS Symfony Extended Range of Vision IOL, Model No. ZXR00 The product is indicated primary implantation for the visual correction of aphakia in adult patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract extraction, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1504-2016·2016-09-28
Sun Pharmaceutical Recalls Carvediol Tablets Due to Impurity Failures
Sun Pharmaceutical Industries is recalling specific lots of Carvediol Tablets because they failed impurity and degradation specifications.
Product
Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count bottle (NDC 57664-242-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2860-2016·2016-09-28
Abbott Recalls SENSAR Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling SENSAR 1-Piece Intraocular Lenses because they were not checked prior to release, which may result in the release of mislabeled units.
Product
SENSAR 1-Piece IOL, Model No. AAB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2852-2016·2016-09-28
Siemens Syngo.x Software Recalled for Incorrect Volume Calculations
Siemens Medical Solutions is recalling 338 Syngo.x PACS systems because a software error caused volume calculations for prostate and liver to be too high.
Product
Syngo.x picture archiving and communication system Syngo.x is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2862-2016·2016-09-28
Abbott Recalls Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 70 units of TECNIS OptiBlue Intraocular Lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS OptiBlue 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00V The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1507-2016·2016-09-28
Sun Pharmaceutical Recalls Carvediol Tablets Due to Impurity Failures
Sun Pharmaceutical Industries is recalling Carvediol Tablets, USP, 25 mg, because the product failed impurities and degradation specifications.
Product
Carvediol Tablets, USP, 25 mg, 100-count bottle (NDC 57664-247-88), 500-count bottle (NDC 57664-247-13), 1000-count bottle (NDC 57664-247-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by: Sun Pharmaceutical…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2856-2016·2016-09-28
Abbott Recalls TECNIS Multifocal Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 77 TECNIS Multifocal Intraocular Lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS Multifocal 1-Piece Intraocular Lens, Model No. ZKB00, ZLB00; The product is indicated for primary implantation for the visual correction of aphakia in adult patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2869-2016·2016-09-28
Hologic Sertera Biopsy Device Recalled for Incorrect Labeling
Hologic is recalling 570 units of the Sertera Biopsy Device due to incorrect labeling on the sterile kit.
Product
Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2399-2016·2016-09-28
Keebler Sugar Wafers Recalled for Foreign Matter in Sugar Ingredient
Shearer's Snacks is recalling Keebler Sugar Wafers, Vanilla, because the refined granulated sugar ingredient contains extraneous foreign matter.
Product
Keebler, Sugar Wafers, Vanilla, Net Wt 2.75 OZ (77 g), Made in Canada Distributed By Kellogg Sales Co, Battle Creek, MI 49016 USA
Category
Food
Distribution
10 states
ModerateFDA (Devices)·Z-2853-2016·2016-09-28
Siemens Syngo.via Software Recalled for Incorrect Volume Calculations
Siemens Medical Solutions is recalling 338 Syngo.via systems because a software error caused volume calculations for prostate and liver to be too high.
Product
Syngo.via picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2861-2016·2016-09-28
Abbott Recalls TECNIS Intraocular Lenses Due to Mislabeled Units
Abbott Medical Optics is recalling 217 TECNIS 1-Piece Intraocular Lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2875-2016·2016-09-28
Pentax Video Bronchoscopes Recalled for Incorrect Operation and Reprocessing Instructions
Pentax of America Inc. is recalling 1,719 video bronchoscopes because they contain an incorrect Operation and Reprocessing IFUS.
Product
Pentax Video Bronchoscope Designed to be used with a Pentax Video Processor (including light source), documentation equipment, video monitor, endo-therapy accessories (such as biopsy forceps) and other ancillary equipment for endoscopy and endoscopic surgery within the airways…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1505-2016·2016-09-28
Sun Pharmaceutical Recalls Carvediol Tablets Due to Impurity Specifications
Sun Pharmaceutical Industries is recalling specific lots of Carvediol Tablets, USP, 6.25 mg, because they failed impurities and degradation specifications.
Product
Carvediol Tablets, USP, 6.25 mg, 100-count bottle (NDC 57664-244-18), 500-count bottle (NDC 57664-244-13), 1000-count bottle (NDC 57664-244-18), Rx Only, Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2843-2016·2016-09-28
OrthoPediatrics Recalls Mislabeled 3.5mm Bowed Locking Compression Femur Plates
OrthoPediatrics Corp is voluntarily recalling 41 units of 3.5mm Bowed Locking Compression Femur Plates due to mislabeling.
Product
3.5mm Bowed Locking Compression Femur Plates, 14 hole Orthopediatrics PediLoc Locking Plate System comes in sets that offer the advantage of both conventional and locking plate fixation devices and instrumentation in one system. Utilizing both locking and non- locking screws…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2858-2016·2016-09-28
Abbott Recalls Mislabeled Intraocular Lenses Due to Quality Control Failure
Abbott Medical Optics is recalling 65 units of TECNIS 1-Piece Intraocular Lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
TECNIS 1-Piece IOL, Model No. ZCB00 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1506-2016·2016-09-28
Sun Pharmaceutical Recalls Carvediol Tablets Due to Impurity Failures
Sun Pharmaceutical Industries is recalling specific lots of Carvediol Tablets, 12.5 mg, because they failed impurities and degradation specifications.
Product
Carvediol Tablets, USP, 12.5 mg, 500-count bottle (NDC 57664-245-13), 1000-count bottle (NDC 57664-245-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2873-2016·2016-09-28
Hospira LifeCare PCA Infusion System Recalled for Screw Rotation Error
Hospira Inc. is recalling 8,794 LifeCare PCA Infusion Systems because a screw rotation error can cause the pump to alarm and stop infusion.
Product
LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2864-2016·2016-09-28
Abbott Recalls Mislabeled Intraocular Lenses Due to Quality Control Failure
Abbott Medical Optics is recalling 41 intraocular lenses because they were not checked prior to release, potentially resulting in mislabeled products.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model No. Z9002 The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2836-2016·2016-09-28
SybronEndo Recalls Sealapex Xpress Root Canal Resin Due to Labeling Error
SybronEndo is recalling 179 units of Sealapex Xpress root canal filling resin because the product was labeled with an incorrect expiration date.
Product
Sealapex Xpress, Part No. 33639 The brand name of the device is Sealapex Xpress, a root canal filling resin. Sealapex Xpress is intended to be used during endodontic therapy to fill the root canal of a tooth.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2865-2016·2016-09-28
Merge Cardio software recall for missing patient information on report pages
Merge Healthcare is recalling Merge Cardio software version 10.1 because patient information is missing from subsequent report pages.
Product
Merge Cardio software. Product Usage: Merge Cardio is an integrated cardiovascular information system classified as a picture archiving and communications system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2844-2016·2016-09-28
OrthoPediatrics Recalls Mislabeled 3.5mm Bowed Locking Compression Femur Plates
OrthoPediatrics Corp is voluntarily recalling 41 units of 3.5mm Bowed Locking Compression Femur Plates due to mislabeling. The devices were distributed nationwide to specific states.
Product
3.5mm Bowed Locking Compression Femur Plates, 18 hole Orthopediatrics PediLoc Locking Plate System comes in sets that offer the advantage of both conventional and locking plate fixation devices and instrumentation in one system. Utilizing both locking and non- locking screws…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2863-2016·2016-09-28
Abbott Recalls 41 Intraocular Lenses Due to Mislabeled Product Risk
Abbott Medical Optics is recalling 41 TECNIS Multifocal Intraocular Lenses because they were not checked prior to release, posing a risk of mislabeling.
Product
TECNIS Multifocal Foldable Acrylic Intraocular Lens, Model No. ZMA00 The product is indicated for primary implantation for the visual correction of aphakia in adult patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2851-2016·2016-09-28
CooperSurgical Recalls Sage CSC Thawing Medium Due to Incorrect Package Insert
CooperSurgical, Inc. is recalling 4 units of Sage CSC Thawing Medium because the products contain an international package insert instead of the correct USA package insert.
Product
Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation) Thawing Medium Product Number: ART-8018 Intended for use in freezing embryos. This product is intended for thawing of embryos frozen with ART-8017, CSC Freezing Medium. This kit is designed to be used in…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Food)·F-2398-2016·2016-09-28
Shearer's Snacks Recalls Family Gourmet Sugar Wafers Due to Foreign Matter
Shearer's Snacks is recalling Family Gourmet Sugar Wafers because an ingredient contained foreign matter. The product was distributed to specific states.
Product
Family Gourmet, Sugar Wafers, Strawberry, Net Wt 8 OZ (227 g), Distributed By: Family Dollar Services, Inc. Charlotte, NC 28201 USA Product of Canada
Category
Food
Distribution
10 states