State

Oklahoma product recalls

73,092 recalls have nationwide distribution and so reach Oklahoma. 5,816 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,816
Critical: 1,043
Severe: 1,250
Most recent: 2026-09-23

Of the 5,816 recalls naming Oklahoma we have scored against our rubric, 1,043 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,250 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,816 recalls whose distribution notice names Oklahoma specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8126–8150 of 78908

SevereFDA (Drugs)·D-0223-2025·2025-02-12
Adrenalin Chloride Epinephrine Nasal Solution Recalled for Misleading Label
Par Pharmaceutical is recalling Adrenalin Chloride Solution (Epinephrine Nasal Solution) due to a misleading label that resembles the FDA-approved Adrenalin epinephrine injection product, creating potential confusion.
Product
Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0533-2025·2025-02-12
Seasoned Bread Crumbs Recalled Due to Undeclared Sesame Allergen
La Fiesta Food Products is recalling seasoned bread crumbs because they contain undeclared sesame, an allergen not listed on the label. The product was distributed nationwide.
Product
La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned, NET WT 8 OZ. (227g), UPC# 032327000887
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1046-2025·2025-02-12
X-Ray Imaging System May Continue Exposure Beyond Safety Limit
GE Medical Systems' Optima XR646 HD X-Ray imaging systems may allow continued radiation exposure beyond the safety limit without operator confirmation. A warning message displays but does not prevent the excess exposure.
Product
Optima XR646 HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1078-2025·2025-02-12
Philips AlluraXper Patient Tables Pose Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion fluoroscopy systems. Manual repositioning can trap fingers between the tabletop and rails, risking injury to operators and service personnel.
Product
AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0460-2025·2025-02-12
Monkey Spit BBQ Sauce recalled for undeclared milk allergen
Monkey Spit Monkey Mop BBQ Sauce is recalled because it contains undeclared milk from butter, a common allergen. Consumers with milk allergies should not consume this product.
Product
Monkey Spit "Monkey Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactured by Smith House MFG. 146-A S. Thompson Ave. Nipomo, CA 93444 (805)619-7959 Monkey Spit, LLC, UPC#8 54540 00206 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0524-2025·2025-02-12
Donut Product Recalled for Potential Listeria Monocytogenes
FGF, LLC is recalling approximately 2 million cases of its BAV CRM BAR DONUT product nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Product
item 8201923 BAV CRM BAR DONUT PFD 78 X 3OZ, NET WT 13.16 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0470-2025·2025-02-12
Cake Donut Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling cake donut rings due to potential contamination with Listeria monocytogenes. Distribution included nationwide US and Canada.
Product
item 8201779 GEN PLN CAKE DONUT RINGS PFD 90x2.5 OZ, NET WT 12.66LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0492-2025·2025-02-12
FGF Frozen Bismark Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling frozen Bismark donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201843 GEN BISMARK DONUT DGH FRZ 144x2OZ, NET WT 16.20 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0525-2025·2025-02-12
Donuts Recalled for Potential Listeria Monocytogenes Contamination
FGF LLC is recalling egg-shaped donuts nationwide due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed in the US and Canada.
Product
item 8201926 FBALL/EGG SHPD DONUT PFD 78 X 2OZ, NET WT 8.78 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0502-2025·2025-02-12
Just Baked Apple Fritters Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling Just Baked Apple Fritters nationwide due to potential Listeria monocytogenes contamination. Consumers should discard affected products.
Product
item 8201865 JUST BAKED APPLE FRITTERS 72x3OZ, NET WT 13.50 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0506-2025·2025-02-12
FGF Fluff Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of item 8201870 Fluff Donuts due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024, and distributed nationwide in the US and Canada.
Product
item 8201870 GEN BAR FLUFF DONUT ZGT PFD 78x3OZ, NET WT 13.16 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0501-2025·2025-02-12
FGF LLC Recalls Just Baked Coffee Rolls Over Listeria Contamination Risk
FGF LLC is recalling 2,017,614 cases of Just Baked Coffee Rolls (78 x 3oz packages) due to potential Listeria monocytogenes contamination. The affected product was produced on or before 12/13/24 and distributed nationwide in the US and Canada.
Product
item 8201864 JUST BAKED COFFEE ROLLS 78x3OZ, NET WT 14.62 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1079-2025·2025-02-12
Philips Allura patient tables recall due to finger entrapment risk
Philips recalls AD7 and AD7X patient tables in Allura and Azurion systems due to finger entrapment risk during manual repositioning. Operators and service personnel could suffer finger injuries.
Product
Allura Xper FD10C System Code: (1) 722001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0485-2025·2025-02-12
Apple-Filled Paczki from FGF, LLC recalled for potential Listeria contamination
FGF, LLC is recalling apple-filled paczki sold nationwide due to potential contamination with Listeria monocytogenes. Affected units were produced on or before December 13, 2024.
Product
item 8201817 APPLE FILLED PACZKI 66x4 OZ, NET WT 14.85 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0491-2025·2025-02-12
Frozen Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling 2,017,614 cases of frozen donuts nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume this product.
Product
item 8201842 GEN BAR DONUT DGH FRZ 132x2OZ, NET WT 14.85 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0480-2025·2025-02-12
French Crullers Recalled Nationwide for Potential Listeria Contamination
FGF, LLC is recalling French Crullers sold nationwide and in Canada due to potential Listeria monocytogenes contamination. All product with expiration dates from 12/13/24 and earlier is affected.
Product
item 8201812 FRENCH CRULLERS 72x 1.6 OZ, NET WT 6.48 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1086-2025·2025-02-12
Philips AD7 and AD7X Patient Table Finger Entrapment Risk
The Philips AD7 and AD7X patient tables pose a finger entrapment risk during manual repositioning. Operators and service personnel could sustain finger injuries from the gap between the longitudinal guiding rails and tabletop.
Product
AlluraXperFD20/15 System Code: (1) 722058
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0517-2025·2025-02-12
FGF Chocolate Cake Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of JUST BAKED Chocolate Cake Rings distributed nationwide in the US and Canada due to potential Listeria monocytogenes contamination.
Product
item 8201904 JUST BAKED CHOCOLATE CAKE RINGS ARTIFICIALLY FLAVORED 144x2.5OZ, NET WT 22.5 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0221-2025·2025-02-12
Potassium Chloride Tablets Recalled for Failed Dissolution Specifications
The FDA is recalling Potassium Chloride Extended-Release Tablets (10 mEq) distributed nationwide because they failed dissolution tests. This could affect how the medication is released in the body.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0527-2025·2025-02-12
FGF LLC Bavarian Bismark pastry items recalled for potential listeria contamination
FGF LLC is recalling Bavarian Bismark pastry item 8201936 due to potential listeria monocytogenes contamination. The recall covers all product within expiration produced on or before December 13, 2024, distributed nationwide in the US and Canada.
Product
item 8201936 NATURAL & ARTIFICIAL FLAVORED BAVARIAN BISMARK, NET WT 13.16 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0481-2025·2025-02-12
FGF Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling dual-filled chocolate and Bavarian yeast ring donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed in the US and Canada.
Product
item 8201813 DUAL FILLED NATURALLY & ARTIFICIALLY FLAVORED CHOCOLATE AND BAVARIAN FILLED YEAST RING DONUT 80x3.1OZ, NET WT 13.97 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0215-2025·2025-02-12
Prescription Carvedilol recalled for manufacturing impurity exceeding FDA specifications
Glenmark Pharmaceuticals is recalling Carvedilol 25 mg tablets nationwide due to a manufacturing quality issue with impurity levels exceeding FDA recommended limits. Multiple lot numbers and expiration dates from February 2025 through February 2026 are affected.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1076-2025·2025-02-12
Philips Allura CV20 patient tables risk finger entrapment during repositioning
The Philips Allura CV20 System patient tables (AD7 and AD7X models) pose a finger entrapment hazard during manual repositioning. Fingers can become caught between the tabletop and guiding rails, potentially injuring operators and service personnel.
Product
Allura CV20 System Code: 722031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1105-2025·2025-02-12
NeiMed NasoGel nasal spray recalled due to stability failure
Neilmed Pharmaceuticals is recalling NasoGel for Dry Noses due to stability failure that may allow microbial growth. The product was distributed across 30 U.S. states and to five countries.
Product
NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL GSP30-SWE-INTL GSP30-ENG-INT GSP30-MAL-INTL GSP30-SPA-INT NasoGel Spray is a saline-based gel formula that can be sprayed to moisturize and lubricate dry and i
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2025·2025-02-12
Philips Azurion and Allura Patient Tables: Finger Entrapment Hazard
Philips patient tables on Azurion and Allura imaging systems can trap fingers between the tabletop and rails during manual repositioning. Operators and service personnel are at risk of finger injury.
Product
Azurion 3 M12 System Code: (1) 722063 (2) 722221
Category
Medical Device
Distribution
Distributed nationwide