State

Oklahoma product recalls

73,738 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,040
Severe: 1,493
Most recent: 2026-10-28

Of the 5,822 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 1,493 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35451–35475 of 79560

ModerateFDA (Devices)·Z-1990-2019·2019-07-31
Abbott Immunoglobulin M Diagnostic Assay Recalled for Instruction Manual Errors
Abbott Laboratories is recalling 9,586 Immunoglobulin M diagnostic kits because the instructions for use contained errors in the reagents and specimen handling sections.
Product
Immunoglobulin M is an in vitro diagnostic assay for the quantitative determination of immunoglobulin M in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1995-2019·2019-07-31
Abbott Transferrin Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 22,359 Transferrin in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
Transferrin is an in vitro diagnostic assay for the quantitative determination of transferrin in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1516-2019·2019-07-31
Amneal Recalls Methylergonovine Maleate Tablets Due to Foreign Tablet Presence
Amneal Pharmaceuticals is recalling specific lots of Methylergonovine Maleate tablets because a Promethazine tablet was found in a bottle.
Product
Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC 69238-1605-02) and b) 28 count bottles (NDC 69238-1605-08)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1497-2019·2019-07-31
Pharma-Natural Recalls GENCONTUSS Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 3,000 bottles of GENCONTUSS cough syrup because it was manufactured with current good manufacturing practice violations.
Product
GENCONTUSS — GENCONTUSS (CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1506-2019·2019-07-31
Pharma-Natural Recalls NEOGEN-D Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 2,052 bottles of NEOGEN-D cough syrup because the product was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
NEOGEN-D (Dextromethorphan HBr, 30 mg; Guaifenesin, 200 mg; Phenylephrine HCl, 7.5 mg) in each 5 mL tsp, Raspberry Flavor, 16 fl oz (473 mL) bottle, Manufactured in the USA for Kramer Novis, San Juan, PR 00917, NDC 52083-699-16.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1991-2019·2019-07-31
Abbott Apolipoprotein A1 Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 2,112 Apolipoprotein A1 assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
Apolipoprotein A1 is an in vitro diagnostic assay for the quantitative determination of apolipoprotein A1 in human serum or plasma. Antibodies to apolipoprotein A1 combine with apolipoprotein A1 in the sample to form insoluble immune complexes. The immune complexes cause an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1499-2019·2019-07-31
Pharma-Natural Recalls LidoAID Gel Due to Manufacturing Violations
Pharma-Natural Inc. is recalling LidoAID topical analgesic gel because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
LidoAID (Lidocaine HCL 4%) portable pain relieving TOPICAL ANALGESIC GEL, 0.17 Oz (4 g) roll on bottle, Distributed by: Diabetic Supply of Suncoast, Inc., dba Advocate Diabetes, PO Box 2102, Vega Alta, PR 00692, NDC 63788-114-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2019·2019-07-31
Epimed Versa-Kath Mini Kit Recalled for Incorrect Catheter Size Labeling
Epimed International is recalling 200 Versa-Kath Mini Kits because the labeling incorrectly states a 12-gauge catheter is included, while the kit actually contains a 21-gauge catheter.
Product
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 311291155 for epidural or caudal anesthesia
Category
Medical Device
Distribution
8 states
ModerateFDA (Drugs)·D-1505-2019·2019-07-31
Pharma-Natural Recalls SORBUGEN Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 7,392 bottles of SORBUGEN cough syrup because the product was manufactured with current good manufacturing practice violations.
Product
SORBUGEN — SORBUGEN (DEXTROMETHORPHAN HYDROBROMIDE, GLYCEROL GUAIACOLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1941-2019·2019-07-31
Ragu Old World Style Sauce Recalled for Foreign Material
Mizkan America is recalling 654 jars of Ragu Old World Style Sauce Flavored with Meat due to the presence of foreign material.
Product
Ragu Old World Style Sauce Flavored with Meat 66oz retail size sold in plastic jar
Category
Food
Distribution
28 states
ModerateFDA (Devices)·Z-1993-2019·2019-07-31
Abbott Haptoglobin Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 5,694 Haptoglobin Assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
The,K -ASSAY HP assay is intended for the quantitative determination of human haptoglobin by immunoturbidimetric assay. The antiserum used in the kit was produced against purified human haptoglobin. The haptoglobin antibody interacts with the haptoglobin in the serum forming…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2024-2019·2019-07-31
Siemens AXIOM Artis dFA Recalled for Power Supply Tolerance Issue
Siemens is recalling 39 AXIOM Artis dFA units because a power supply issue may cause generator failure, preventing X-ray production during procedures.
Product
AXIOM Artis dFA, Model Number 7555373
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1508-2019·2019-07-31
FDA Recalls Temozolomide Capsules Due to Cross-Contamination Risk
Deva Holding AS is recalling Temozolomide capsules because manufacturing deviations allowed possible cross-contamination with beta-lactam products.
Product
TEMOZOLOMIDE — TEMOZOLOMIDE (TEMOZOLOMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1504-2019·2019-07-31
Pharma-Natural Recalls Tusslin Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling Tusslin cough syrup because it was manufactured with current good manufacturing practice violations, including a lack of process validation.
Product
TUSSLIN (Dextromethorphan HBr, 28 mg; Guaifenesin, 388 mg; Phenylephrine HCl, 10 mg) in each 5 mL tsp, Grape Flavor, 16 Fl.oz. (474 mL) bottle, Kramer Novis, San Juan, PR 00917, NDC 52083-622-16.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2017-2019·2019-07-31
Siemens AXIOM Artis dBC X-ray System Recalled for Power Supply Issue
Siemens is recalling one AXIOM Artis dBC X-ray system because a power supply defect may prevent X-ray generation during procedures.
Product
AXIOM Artis dBC, Model Number 5917054
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2033-2019·2019-07-31
Siemens Artis zee Biplane Recalled for Power Supply Tolerance Issue
Siemens Medical Solutions is recalling three Artis zee biplane MN units due to a power supply tolerance issue that may prevent X-ray generation during procedures.
Product
Artis zee biplane MN, Model Number 10094143
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2013-2019·2019-07-31
Siemens AXIOM Artis FA X-ray Generator Recall for Power Supply Issue
Siemens is recalling four AXIOM Artis FA units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Product
AXIOM Artis FA, Model Number 5904441
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1492-2019·2019-07-31
Pharma-Natural Recalls Oliver's Harvest CBD+Capsaicin Cream for CGMP Violations
Pharma-Natural Inc. is recalling 998 bottles of Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief Cream due to current good manufacturing practice violations.
Product
Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief (Capsaicin 0.2%) Topical Analgesic Cream, 4 OZ (113.4 g) bottle with pump, Distributed by: Coast to Coast Natural, Inc., Wellington, FL 33414, NDC 63788-120-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1503-2019·2019-07-31
Pharma-Natural Recalls Dayma Pain Gel for Manufacturing Violations
Pharma-Natural Inc. is recalling 1,000 jars of Dayma SUPER FORTE XL10 Pain Relieving Topical Analgesic Gel due to current good manufacturing practice violations.
Product
Dayma SUPER FORTE XL10 (Camphor 0.5%, Menthol 2%, Methyl Salicylate 2%) Pain Relieving Topical Analgesic Gel, 4 Oz (113.4 g) jar, Distributed by: Biosfera International Distribution, LLC., Miami Lakes, FL 33016, NDC 63788-118-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2016-2019·2019-07-31
Siemens AXIOM Artis BA X-ray Systems Recalled for Power Supply Defect
Siemens is recalling seven AXIOM Artis BA X-ray systems because a power supply defect may cause the generator to fail, preventing X-ray imaging.
Product
AXIOM Artis BA, Model Number 5904656
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1987-2019·2019-07-31
Abbott C3 In Vitro Diagnostic Assay Recall for Instruction Manual Update
Abbott Laboratories is recalling 8,132 C3 in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
C3 is an in vitro diagnostic assay for the quantitative determination of C3 in human serum or plasma. Antibodies to C3 combine with C3 in the sample to form insoluble immune complexes. The immune complexes cause an increase in light scattering (turbidity). The resulting…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2078-2019·2019-07-31
Abbott Recalls ARCHITECT BNP Calibrators Due to Stability Drift
Abbott Laboratories is recalling 5,483 units of ARCHITECT BNP Calibrators worldwide due to a time-dependent stability drift that affects patient and control test results.
Product
ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem when used for the quantitative determination of human Btype natriuretic peptide (BNP) in human EDTA plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1496-2019·2019-07-31
Pharma-Natural Recalls Army Health Pain Reliever Gel Due to CGMP Violations
Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.
Product
ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%), 0.5 OZ jar, Manufactured exclusively for: Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00461 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2069-2019·2019-07-31
Epimed Versa-Kath Mini Kit Recalled for Incorrect Catheter Size Labeling
Epimed International is recalling 98 Versa-Kath Mini Kits because the labeling incorrectly states the kit contains a 12-gauge catheter, while it actually contains a 21-gauge catheter.
Product
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 31129344 for epidural or caudal anesthesia
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-2061-2019·2019-07-31
Medela Breast Milk Transfer Lid Recall for Packaging Sterility Concerns
Medela Inc is recalling 665,600 breast milk transfer lids because packaging breaches may compromise sterility, even if the packaging appears intact.
Product
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Category
Medical Device
Distribution
Distributed nationwide