State
73,806 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
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.
Cook Inc. is recalling 615 units of Mallinckrodt Institute Percutaneous Gastrostomy Sets because wire guides may be loaded backwards into the holder.
Oakworks Inc. is recalling foot controls for specific medical imaging tables because they can become lodged under the table base or column.
Otto Bock is recalling 75 Kenevo knee joints due to a design issue that could cause the pylon to break under specific heavy-use conditions.
Accord Media, LLC is recalling 524 Ultra Renew devices distributed nationwide because they use an unapproved green LED light to treat hyperpigmentation.
Topson Downs is recalling Cat & Jack Girls' Star Studded Skinny Jeans because metal stars can detach and cause lacerations. Consumers should stop wearing them and return them to Target for a refund.
Zimmer Biomet is recalling 3,350 units of the Segmental System, ZSS Distal Femur, because the products exceeded tested weights, potentially compromising the sterile barrier.
Cook Inc. is recalling Wills-Oglesby Percutaneous Gastrostomy Sets because wire guides may be loaded backwards into the holder.
Philips is recalling 705 Allura Xper systems because Anode Drive Units may fail in high-voltage regions, reducing X-ray performance to emergency mode.
Otto Bock is recalling four Kenevo knee joints due to a design issue that could cause the pylon to break, leading to a fall.
Integra LifeSciences is recalling 155 CUSA Clarity footswitches because a defect may cause unintended ultrasonic fragmentation activation during surgery.
M&P Food Productions is recalling Vareniki Potato and Onion because the product contains undeclared wheat. This poses a risk to individuals with wheat allergies or celiac disease.
Zevex Incorporated is recalling specific lots of Moog Curlin Infusion Administration Sets due to particulate matter found on the spike.
Husqvarna is recalling approximately 160 FS 450 closed course competition motorcycles from model years 2016 to 2018 because a cracked front brake piston can cause brake failure and crashes.
First Aid Research is recalling Maximum Strength Bacitraycin Plus Ointment with Lidocaine because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.
Zevex Incorporated is recalling Moog Curlin Infusion Administration Sets because particulate matter was found on the spike. The recall covers 7,979 cases distributed nationwide and internationally.
Stryker Communications is recalling 850 Berchtold Chromophare Dual Monitor Carrier Arms and Flat Panels because the mounts may have missing or incomplete welds.
Daimler Trucks North America is recalling 2007-2018 Thomas Built Buses Minotour school buses because the wheelchair lift may operate while the vehicle is in motion.
ConMed is recalling STAT 2 I.V. Gravity Flow Needle-Free Controller sets because they exhibit inaccurate or inconsistent flow rates.
M&P Food Productions is recalling Vareniki - farmer cheese due to undeclared wheat. Consumers with celiac disease or wheat allergies should not consume the product.
M&P Food Productions is recalling Vareniki Sour Cherry because the product contains undeclared wheat and Red #40.
BMW is recalling 2018 X3 xDrive30i and M40i vehicles because the rear spoiler may not be properly attached or may be missing screws, posing a road hazard.
Hitachi Medical Systems America Inc is recalling 55 ultrasound transducers (Model UST-5550-R) because they may not have adequate protection against electrical shock hazards.
M&P Food Productions is recalling Vareniki Cabbage because the product contains undeclared wheat. Consumers with celiac disease or wheat allergies should not eat the product.
M&P Food Productions is recalling Hand Made Russian Style Blintzes because they contain undeclared wheat. Consumers should check their pantries for the affected product.
LifeCell is recalling 25,798 units of the Revolve Advanced Adipose System due to bacterial endotoxin levels above acceptable limits.