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.

41976–42000 of 79629

SevereFDA (Drugs)·D-0697-2018·2018-05-02
Bayer Recalls Alka-Seltzer Plus Packages Due to Ingredient Label Mismatch
Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.
Product
All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1531-2018·2018-05-02
BD Vacutainer Push Button Blood Collection Set Recalled for Sterility Failure
Becton Dickinson & Company is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Product
BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12 (Catalog no 367342)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1505-2018·2018-05-02
Stryker T4 Zipper Toga sterile garments recalled for layer separation
Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, creating a risk of exposure to contaminants.
Product
T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2018·2018-05-02
Zimmer Biomet Recalls Pressure Sentinel Guide Wires Due to Sterile Seal Failure
Zimmer Biomet is recalling 19,483 Pressure Sentinel Intramedullary Reaming System Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Product
Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4 mm Diameter; Item Number: 00-2228-024-00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2018·2018-05-02
Zimmer Biomet Recalls Natural Nail System Guide Wires Due to Sterile Seal Failure
Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 100 cm Length; Diameter; Item Number: 47-2490-097-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1487-2018·2018-05-02
Integra LifeSciences Recalls TCC-EZ Total Contact Cast System
Integra LifeSciences is recalling 250 units of the TCC-EZ Total Contact Cast System because a quarantined lot may produce excessive heat.
Product
TCC-EZ, Total Contact Cast System, Model No. TCC2-4051
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1130-2018·2018-05-02
MMRF Neyyappam Recalled for Undeclared Milk Allergen
Maharaja Food Importers is recalling frozen MMRF Neyyappam because the label lists ghee but fails to declare milk, a major allergen.
Product
MMRF Neyyappam, UPC: 870400000111, Frozen
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1129-2018·2018-05-02
MMRF Kumbiliappam Recalled for Undeclared Milk Allergen
Maharaja Food Importers is recalling frozen MMRF Kumbiliappam because the label lists ghee but fails to declare milk as an ingredient.
Product
MMRF Kumbiliappam, UPC: 87040000104, Frozen
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0725-2018·2018-05-02
Coastal Meds Recalls Methylcobalamin Injectable Due to Particulate Matter
Coastal Meds, LLC. is recalling 4,524 vials of Methylcobalamin Injectable due to the presence of unknown particulate matter.
Product
METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1523-2018·2018-05-02
Sofradim Versatex Monofilament Mesh Recalled for Hernia Recurrence Reports
Sofradim Production is recalling Versatex Monofilament Mesh due to patient reports of abdominal hernia recurrence following repair. The firm has updated instructions to warn surgeons about risks in specific procedures.
Product
Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional monofilament polyester textile. Its intended use is for the repair of abdominal wall hernias or other fascial deficiencies that require the addition of a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2018·2018-05-02
Stryker T5 Zipper Toga Sterile Garment Recall for Layer Separation
Stryker is recalling T5 Zipper Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Product
T5 Zipper Toga with Peel-Away Face Shield, (L/XL); Catalog number: 0400-820-100 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0721-2018·2018-05-02
FDA Recalls LIPO-DEN Injectable Due to Unknown Particulate Matter
Coastal Meds, LLC. is recalling 1,309 vials of LIPO-DEN Injectable-30 mL because of the presence of unknown particulate matter.
Product
LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·18V274000·2018-05-02
Winnebago Recalls 2018-2019 RVs Due to Roof Rack Fastener Defect
Winnebago is recalling 293 recreational vehicles because roof racks may detach due to incorrect fasteners, creating a road hazard.
Product
WINNEBAGO — WINNEBAGO ERA, REVEL, TRAVATO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1500-2018·2018-05-02
Stryker T4 Pullover Toga Recalled for Potential Material Separation
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Product
T4 Pullover Toga, (S/M); Catalog Number: 0400-710-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1510-2018·2018-05-02
Stryker T5 Zipper Toga Sterile Garment Recall for Layer Separation
Stryker is recalling T5 Zipper Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Product
T5 Zipper Toga with Peel-Away Face Shield, (XL/T); Catalog number: 0400-850-100 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1476-2018·2018-05-02
Zimmer Biomet Recalls ZMS Intramedullary Fixation Smooth Guide Wires
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.
Product
ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-038-00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1468-2018·2018-05-02
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires due to a potential failure of the sterile packaging seal.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 70 cm length; Item Number: 47-2490-098-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1528-2018·2018-05-02
EEA Hemorrhoid Stapler Recalled for Potential Welding Defect
FDA is recalling EEA Hemorrhoid and Prolapse Stapler Sets due to a potential welding defect that could cause bleeding or anastomotic leak.
Product
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM, Product Number HEM3348, GTIN Number 1 - 10884521047563, GTIN Number 2 - 20884521047560 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1465-2018·2018-05-02
Zimmer Biomet Recalls Humeral Guide Wires Due to Packaging Seal Failure
Zimmer Biomet is recalling 19,483 M/DN Intramedullary Fixation Humeral Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Product
M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only; Item Number: 00-2255-025-00
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18E029000·2018-05-02
FiTech Fuel Injection Systems Recalled for Fuel Leak Fire Risk
Fuel Injection Technology is recalling Summit Racing Max 500-EFI systems because fuel injector O-rings may leak, increasing fire risk.
Product
FUEL SYSTEM, GASOLINE:FUEL INJECTION SYSTEM recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1128-2018·2018-05-02
Maharaja Food Importers Recalls Jack Fruit for Undeclared Milk Allergen
Maharaja Food Importers is recalling ELA ADA (Jack Fruit) because the label lists ghee but fails to declare milk, a major allergen.
Product
ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2018·2018-05-02
BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results
BioFire Diagnostics is recalling the FilmArray BCID Panel because it may produce false positive Proteus results when used with specific BD BACTEC blood culture bottles.
Product
FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catalog numbers 442020, 442021, 442023, 442192, 442265, 442194, 442022, 442193…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2018·2018-05-02
Synthes Stem Extractor Recalled Due to Potential Screw Breakage
Synthes, Inc. is recalling 31 Stem Extractor f/Guide Bar units because the connection screw may break during use.
Product
Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1131-2018·2018-05-02
Frozen Parotta Recalled for Undeclared Milk Allergen
Maharaja Food Importers is recalling frozen Parotta products because the label lists ghee but fails to declare milk, a major allergen.
Product
Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2018·2018-05-02
Stryker T4 Zipper Toga Recall Due to Material Separation Risk
Stryker is recalling T4 Zipper Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.
Product
T4 Zipper Toga, X-Large; Catalog number: 0400-850-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide