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.

50601–50625 of 79640

HighFDA (Devices)·Z-2817-2016·2016-09-21
ICU Medical Recalls Transpac IV Transducer Kits Due to Leak Risk
ICU Medical is recalling 110 units of Double Kit with SafeSet and 03mL Flush Device due to a potential for leak.
Product
Double Kit with SafeSet and 03mL Flush Device, Item No. 46080-37 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2177-2016·2016-09-21
Mars Recalls Combos Pepperoni Pizza Crackers for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Pepperoni Pizza Crackers due to the potential for undeclared peanut residue. The recall affects 183,678 cases distributed nationwide and in foreign markets.
Product
COMBOS PEPPERONI PIZZA CRACKER - Net Wt. 1.70 OZ (48.2 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419714737
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2123-2016·2016-09-21
Hostess Donettes Maple Glazed Mini Donuts Recalled for Peanut Allergen
Hostess Brands is recalling Donettes Maple Glazed Mini Donuts because the product contains peanut allergen but is not labeled to contain peanuts.
Product
Hostess Donettes Maple Glazed Mini Donuts, packaged in 9-17-ct bagsof mini donuts, net wt. 10.50oz, UPC 888109111243; the most responsible firm name on the label is Hostess Brands LLC, Kansas City, MO 64141.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2800-2016·2016-09-21
Siemens RAPIDLab 1240 Blood Gas Analyzer Recalled for Patient Data Mismatch
Siemens is recalling 144 RAPIDLab 1240 Blood Gas Analyzers because patient names may be printed with data from a different patient.
Product
Siemens RAPIDLab 1240 Blood Gas Analyzer Siemens Material Number (SMN): 10321840, 10491392
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2175-2016·2016-09-21
Mars Recalls Combos Pretzels for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Buffalo Blue Cheese Pretzels due to potential undeclared peanut residue.
Product
COMBOS SNACK BUFFALO BLUE CHEESE PRETZEL - Net Wt. 1.80 (51 g) oz Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419474303
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2812-2016·2016-09-21
ICU Medical Recalls Transpac IV Trifurcated Monitoring Kits Due to Leak Risk
ICU Medical is recalling 760 Transpac IV Trifurcated Monitoring Kits because of a potential for leaks in the SafeSet Reservoir and blood sampling components.
Product
Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir and 2 Blood Sampling Ports, 84", 3.3mL Squeeze Flushes, 3 Disposable Transducers, Macrodrip (Pole Mount), Item No. 42650-06 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2819-2016·2016-09-21
ICU Medical Recalls SafeSet Reservoir Kits Due to Potential Leak
ICU Medical is recalling 125 SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Product
SafeSet Kit with 30 mL Flush Device, Item No. 46083-42 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2172-2016·2016-09-21
Mars Recalls Combos Cheddar Cheese Crackers for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Cheddar Cheese Crackers due to potential undeclared peanut residue.
Product
COMBOS SNACKS CHEDDAR CHEESE CRACKER - 15 OZ Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419780497
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2815-2016·2016-09-21
ICU Medical Recalls SafeSet Reservoir Kits Due to Potential Leak
ICU Medical is recalling 10 units of SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Product
Monitoring Kit with 30mL Flush Device, Item No. 46076-15 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2787-2016·2016-09-21
Howmedica Recalls AccuLIF PL Cages Due to Height Reduction
Howmedica Osteonics Corp. is recalling AccuLIF PL Cages because some implants have shown a reduction in height greater than 1 mm after surgery.
Product
AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2823-2016·2016-09-21
ICU Medical Recalls SafeSet Reservoir and Blood Sampling Kits
ICU Medical is recalling specific SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.
Product
Monitoring Kit with TP4, 30 ml Squeeze Flush and Needleless Valve, Item No. 46103-22 Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2166-2016·2016-09-21
Mars Recalls Combos Pizzeria Pretzels for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Pizzeria Pretzels due to potential undeclared peanut residue. The recall covers 183,678 cases distributed nationwide and abroad.
Product
COMBOS PIZZERIA PRETZEL - Net Wt. 6.30 Oz. (178.6 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419420065
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2117-2016·2016-09-21
Hostess Zingers Raspberry Recalled for Unlabeled Peanut Allergen
Hostess Brands is recalling Zingers Raspberry cakes because they were made with flour containing peanut allergen but are not labeled to contain peanuts.
Product
Iced Raspberry cake with creamy filling, packaged as Hostess Zingers Raspberry in 10-ct multi-packs of individual cakes, net wt. 13.40oz (360 g), UPC 888109110604; 6-ct. single serving fun size snack packs, 3 cakes per pack net wt. 4.02oz. (108g), UPC 888109010089; with the…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2782-2016·2016-09-21
Trinity Biotech Captia Measles IgM Test Kit Recalled for QC Failure
Clark Laboratories is recalling specific lots of the Captia Measles IgM test kit because the product failed quality control stability testing.
Product
Trinity Biotech Captia Measles IgM, REF/Product Code 2326060,Test Kit for 96 Determinations, IVD
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2780-2016·2016-09-21
Mentor Artoura Breast Tissue Expander Recall for Packaging Error
Mentor Texas, LP. is recalling 48 Artoura Breast Tissue Expanders because CPX4 devices may have been packaged in Artoura boxes.
Product
Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders can be used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision and tissue defect procedures. The devices are intended for temporary subcutaneous or sub…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2781-2016·2016-09-21
Mentor CPX4 Breast Tissue Expander Recall Due to Packaging Error
Mentor Texas, LP. is recalling 30 units of CPX4 Breast Tissue Expanders because they may have been packaged in the wrong box.
Product
CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue expanders can be used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision and tissue defect procedures. The devices are intended for temporary subcutaneous or sub muscular…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2246-2016·2016-09-21
Kill Cliff Strawberries & Cream Protein Bars Recalled for Potential Mold
Kill Cliff is recalling Strawberries & Cream Protein Bars because they may contain mold. The recall started on June 21, 2016.
Product
KC (Kill Cliff) Strawberries & Cream Protein Bars, 2.1oz (60g) individually wrapped bar (in cases of 12-2.1 oz (60g) bars).
Category
Food
Distribution
40 states
ModerateFDA (Devices)·Z-2777-2016·2016-09-21
Integra Meshed Dermal Regeneration Template Recalled for Calculation Error
Integra LifeSciences is recalling 14 packages of Meshed Dermal Regeneration Template due to an incorrect calculation of peel strength test results.
Product
Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 in x 2in) Rx Only Meshed Integra¿ Dermal Regeneration Template, (Integra template) is a bilayer membrane system for skin replacement. The dermal replacement layer is made of a porous matrix of fibers of cross-linked…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1501-2016·2016-09-21
Amerisource Recalls bupropion Hydrochloride Tablets for Dissolution Failure
Amerisource Health Services is recalling 2,626 bottles of bupropion hydrochloride extended-release tablets due to failed dissolution specifications.
Product
buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories, NDC 68001-264-03
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2793-2016·2016-09-21
Siemens Syngo Plaza PACS Recall for Measurement Display Suffix
Siemens is recalling 101 Syngo Plaza PACS systems because a suffix on DICOM images may indicate that displayed measurements differ from actual values.
Product
Syngo Plaza picture archiving and communication system (PAC) (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2770-2016·2016-09-21
Sysmex Fluorocell PLT Reagent Recalled for Potential Low Platelet Results
Sysmex America Inc is recalling Fluorocell PLT reagent because it may produce falsely low platelet results on Sysmex XN-Series analyzers.
Product
Fluorocell PLT reagent, Catalog #CD994563 Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology analyzers
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2794-2016·2016-09-21
Siemens Syngo.Plaza VB 10 A PACS Recall for Measurement Suffix Display
Siemens is recalling 101 Syngo.Plaza VB 10 A image processing systems because a suffix on DICOM images may indicate that displayed measurement values differ from real values.
Product
Syngo.Plaza VB 10 A, image processing system (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2804-2016·2016-09-21
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Calibrator Kit 31
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 31, Lot 3155, because an incorrect value on the Assay Data Disks prevents successful calibration of the HbA1c assay.
Product
The VITROS¿ Chemistry Products Calibrator Kit 31, Lot 3155 used in conjunction with: VITROS¿ Chemistry Products HbA1c Reagent Kit, Generation 6 (GEN 6) and Assay Data Disk (ADD), Data Release Versions (DRV) 5873, 5874, 5875, or 5876, is used to calibrate the VITROS 5,1 FS…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2779-2016·2016-09-21
Biomerieux Recalls VIDAS NT-pro-BNP Kits Due to Packaging Error
Biomerieux is recalling 229 VIDAS NT-pro-BNP kits because they contain the incorrect number of control vials.
Product
VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2778-2016·2016-09-21
Alere LDX Optical Check Cassettes Recalled for Incorrect Expiration Date
Alere San Diego, Inc. is recalling LDX Optical Check Cassettes because the expiration date on the magnetic strip does not match the labeled date.
Product
LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Cassette in box with foam insert. The cassette is used to check the optics system of the LDX analyzer. Product Usage: The Optics Check Cassette is used to check the optics system of the Alere Cholestech…
Category
Medical Device
Distribution
Distributed nationwide