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.

50651–50675 of 79640

SevereFDA (Drugs)·D-1489-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Extended-Release Capsules
Amerisource Health Services is recalling 115 cartons of 25 mg amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 25 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1482-2016·2016-09-14
Amerisource Recalls Mispackaged Amphetamine Tablets Due to Unit Dose Errors
Amerisource Health Services is recalling 2,276 cartons of 10 mg amphetamine tablets because blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 10 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2717-2016·2016-09-14
Aribex Recalls NOMAD Pro2 X-Ray Systems Due to Battery Fire Risk
Aribex Inc is recalling 16,871 NOMAD Pro2 X-Ray systems because internal lithium-ion batteries may short-circuit, causing overheating, smoke, or ignition.
Product
NOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged X-Ray System Black, Part Number 08500022; NOMAD Pro2 Vet Packaged X-Ray System, Part Number 08500023; NOMAD Pro2 Vet Packaged X-Ray System Black, Part Number 08500024; NOMAD Pro2 Packaged X-Ray System…
Category
Medical Device
Distribution
52 states
SevereFDA (Devices)·Z-2716-2016·2016-09-14
Aribex Recalls NOMAD Pro X-Ray Systems Due to Battery Fire Risk
Aribex Inc is recalling NOMAD Pro X-Ray systems because internal lithium-ion batteries may short-circuit, causing overheating, melting, smoking, or ignition.
Product
NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD Pro Packaged X-Ray System - Europe, Part Number 08500013; NOMAD Pro X-Ray System, Remote Config., Part Number 08500017; NOMAD Pro Packaged X-Ray System JP…
Category
Medical Device
Distribution
52 states
SevereFDA (Drugs)·D-1495-2016·2016-09-14
Teva Recalls Linezolid Injection Due to Manufacturing Deviations
Teva North America is voluntarily recalling 92,480 containers of Linezolid Injection 600 mg/300 mL due to CGMP deviations. The recall covers products distributed nationwide and in Puerto Rico.
Product
Linezolid Injection 600 mg/300 mL Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-9060-31- (Single Use Container), NDC# 0703-9060-33 (Box of 10 Singe Use Containers)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V662000·2016-09-14
Gillig Recalls 2014-2016 Low Floor Buses Due to Brake Hose Fraying
Gillig is recalling 2014-2016 Low Floor transit buses because rear brake hoses can fray, potentially causing brake lockup or failure and increasing crash risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2768-2016·2016-09-14
Bayer Certegra Workstation Recalled for Fire and Smoke Risk
Bayer Healthcare is recalling 165 Certegra Workstations used with Medrad Stellant CT Injection Systems because they may produce smoke and sparks of fire.
Product
Certegra Workstation used in conjunction with Medrad Stellant CT Injection System Catalog Number # CWKS DISPLAY Serial Numbers The Medrad Stellant CT Injector System is intended for the specific purpose of injecting intravenous contrast media into humans for diagnostic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2069-2016·2016-09-14
Nature Made Adult Gummies Recalled for Possible Salmonella Contamination
Pharmavite is recalling specific lots of Nature Made adult gummies due to possible Salmonella contamination. Consumers should check lot numbers and stop using the product.
Product
Nature Made(R) adult gummies Multi for Her plus Omega-3, 150 count, UPC 0-31604-04275-2
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2080-2016·2016-09-14
Lysander's Spicy Bourbon Rub Recalled for Undeclared Soy and Wheat Allergens
Geneva Foods is recalling Lysander's All Natural Spicy Bourbon Flavor Rub because it contains undeclared soy and wheat allergens and does not declare sulfites.
Product
Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g) foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2099-2016·2016-09-14
Dannon Recalls Activia Fiber Yogurt Due to Incorrect Gluten-Free Labeling
The Dannon Company is recalling Activia FIBER Lowfat Yogurt because the packaging displays a Certified Gluten-Free mark despite containing wheat.
Product
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill seal plastic cups
Category
Food
Distribution
33 states
HighFDA (Devices)·Z-2722-2016·2016-09-14
Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm
Hospira Inc. is recalling 357,778 Plum A+ Hyperbaric Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruptions.
Product
Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2736-2016·2016-09-14
Philips BrightView XCT Gamma Camera Recalled for Software Defect
Philips Medical Systems is recalling 424 BrightView XCT gamma cameras due to a software defect that may cause the detector to contact patients during specific scans.
Product
BrightView XCT Model 882482, gamma camera for Single Photon Emission Computed Tomography (SPECT)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2745-2016·2016-09-14
Smith & Nephew Whipknot Soft Tissue Cinch Suture Recalled for Sterility Breach
Smith & Nephew is recalling Whipknot Soft Tissue Cinch sutures because sterile packaging was breached, compromising sterility. The recall covers 34,065 units distributed worldwide.
Product
Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: 7211015 Used during ligament reconstruction.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16262·2016-09-14
Zeagle Buoyancy Control Devices Recalled for Drowning Hazard
Huish Outdoors is recalling Zeagle Grace and Element BCDs because they may leak air, causing loss of flotation and posing a drowning risk to scuba divers.
Product
Zeagle brand buoyancy control devices (BCDs)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2761-2016·2016-09-14
Riverpoint Medical Recalls Nylon Surgical Sutures Due to Seal Integrity Issues
Riverpoint Medical is recalling sterile nylon surgical sutures because the seals may become open during distribution or packaging.
Product
Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2728-2016·2016-09-14
Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm
Hospira is recalling 357,778 Plum A+3 Infusion Pump Systems because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.
Product
Plum A+3 Infusion Pump System. List Number 12348. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2068-2016·2016-09-14
Nature Made Gummy Multivitamin Recalled for Possible Salmonella Contamination
Pharmavite is recalling specific lots of Nature Made adult gummy multivitamins due to possible Salmonella contamination. Consumers should check their lot numbers and expiration dates.
Product
Nature Made(R) adult gummies Multi for Her plus Omega-3, 100 count, UPC 0-31604-04236-3
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2098-2016·2016-09-14
McCain Foods Recalls Fire Roasted Poblano and Jalapeno Popper Bites
McCain Foods USA is recalling Fire Roasted Poblano & Jalapeno popper bites because the flour used was contaminated with E. Coli O121.
Product
Fire roasted Poblano & Jalapeno popper bites packaged in a white box with black lettering. The product is labeled in part: Canchor Poppers Fire Roasted & Jalapeno popper bites, 2-4 lbs.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2724-2016·2016-09-14
Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm
Hospira is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and delay or interrupt therapy.
Product
Plum A+ Infusion Pump. List Number 11973. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2721-2016·2016-09-14
Elekta Medical Linear Accelerator Recall for Loose Drive Gear Joint
Elekta is recalling 553 Medical Linear Accelerators because a loose joint between the drive gear and gantry base drive wheel can lead to fatigue failure of securing bolts.
Product
Medical Linear Accelerator
Category
Medical Device
Distribution
20 states
HighFDA (Devices)·Z-2730-2016·2016-09-14
Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm
Hospira is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.
Product
Plum A+3 Infusion Pump with Hospira MedNet Software. List Number 20678. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2750-2016·2016-09-14
Hill-Rom Recalls 94 Affinity Four Birthing Beds Due to Defect
Hill-Rom is voluntarily recalling 94 Affinity Four Birthing Beds (Model P3700) distributed in the US and abroad. The recall was initiated by the firm.
Product
Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace, standard corrugated cardboard and plastic banding. When possible these beds are shipped as a quantity of two (2) together as shown with the nylon strapping.…
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-2723-2016·2016-09-14
Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm
Hospira Inc. is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.
Product
Plum A+ Infusion Pump. List Number 11971. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1485-2016·2016-09-14
Amerisource Recalls Mispackaged Amphetamine Tablets Due to Dosing Errors
Amerisource Health Services is recalling 156 cartons of 30 mg amphetamine tablets because blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2726-2016·2016-09-14
Hospira Recalls Plum A+ Infusion Pumps Due to Undersized Diaphragm
Hospira Inc. is recalling 357,778 Plum A+ Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.
Product
Plum A+ Infusion Pump with Hospira MedNet Software. List Number 20679. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are…
Category
Medical Device
Distribution
Distributed nationwide