State

Oklahoma product recalls

73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,824
Critical: 1,040
Severe: 1,494
Most recent: 2026-11-14

Of the 5,824 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 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56701–56725 of 79657

CriticalFDA (Drugs)·D-1351-2015·2015-09-02
Teva Recalls ADRUCIL Fluorouracil Injection Due to Particulate Matter
Teva Pharmaceuticals USA is recalling ADRUCIL (fluorouracil injection) vials due to the presence of silicone rubber and fluorouracil crystals in the solution.
Product
ADRUCIL (fluorouracil injection, USP), 5 g/100 mL (50 mg/mL) glass vials, 5 x 100 ml vials per carton, manufactured by Teva Parenteral Medicines, Inc., Irvine, CA. NDC 073-3019-11 (individual vial), NDC 0703-3019-12 (carton of five).
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1357-2015·2015-09-02
PharMEDium Recalls Heparin Sodium Injection Bags Due to Particulate Matter
PharMEDium Services, LLC is recalling 240 bags of Heparin Sodium Injection USP 25,000 Units in 250 mL bags due to the presence of particulate matter.
Product
HEPARIN Sodium Injection USP 25,000 USP Units added to 250 mL 5% Dextrose Injection USP (100 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0419, NDC# 61553-419-02.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1356-2015·2015-09-02
PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter
PharMEDium Services, LLC is recalling 48 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.
Product
EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Chloride Injection USP (64 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6618, NDC# 61553-618-61.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1358-2015·2015-09-02
PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter
PharMEDium Services, LLC is recalling 264 bags of Epinephrine HCl injection due to the presence of particulate matter in the saline solution.
Product
EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Chloride Injection USP (16 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6119, NDC# 61553-119-61.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1354-2015·2015-09-02
PharMEDium Recalls Epinephrine Injection Bags Due to Particulate Matter
PharMEDium Services is recalling 36 bags of Epinephrine HCl injection due to the presence of particulate matter in the solution.
Product
EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Chloride Injection USP (4 mcg per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K6244, NDC# 61553-244-61.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1365-2015·2015-09-02
Mucinex Fast-Max Cold & Sinus Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast-Max Cold & Sinus liquid because the back of the bottle is missing active ingredients and safety warnings.
Product
Mucinex Fast-Max Cold & Sinus, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Ages 12+, Dist. by: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1363-2015·2015-09-02
Mucinex Fast-Max Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Product
MUCINEX FAST-MAX — MUCINEX FAST-MAX (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1366-2015·2015-09-02
Mucinex Fast-Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu Two - 6 fl oz (180 mL) bottles Total -12 fl oz (360 mL), For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-526-22
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1364-2015·2015-09-02
Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast Max Night Time Cold & Flu liquid bottles because the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Night Time Cold & Flu, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Diphenhydramine HCl Antihistamine/Cough Suppressant, Phenylephrine HCl Nasal Decongestant, 6 fl oz. (180 mL) Bottle, For Ages 12+, Dist. By: Reckitt Benckiser Parsippany, NJ…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1367-2015·2015-09-02
Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles where the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Severe Congestion & Cough, Maximum Strength, Dextromethorphan HBr Cough Suppressant, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1361-2015·2015-09-02
GlaxoSmithKline Recalls Bactroban Cream Due to Penicillin Contamination
GlaxoSmithKline is recalling Bactroban Cream (mupirocin calcium) 2% because the product was contaminated with penicillin and foreign substances during manufacturing.
Product
Bactroban Cream (mupirocin calcium), 2%, a) 15g tube ( NDC 0029-1527-22), b) 30g tube (NDC 0029-1527-25), Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2374-2015·2015-09-02
Ethicon Recalls SEDASYS Sedation Systems Due to Plastic Degradation
Ethicon is recalling 14 SEDASYS Computer-Assisted Personalized Sedation Systems because unspecified disinfecting methods caused the plastic material of the Control Unit to degrade.
Product
SEDASYS Computer-Assisted Personalized Sedation System, SEDPRU01. An integrated physiological monitoring and drug delivery system intended to provide physician-led teams with a means of administering 1% propofol (10 mg/mL) injectable emulsion to sedate patients > 18 (ASA…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1359-2015·2015-09-02
Bactroban Nasal Ointment Recalled for Penicillin Contamination
GlaxoSmithKline is recalling Bactroban Nasal Ointment due to penicillin cross-contamination and foreign substances found during manufacturing.
Product
Bactroban (mupirocin calcium) Nasal Ointment, 2% 1g tube, Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217. NDC 0029-1526-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1368-2015·2015-09-02
Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles because the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu, Maximum Strength, Two - 6 fl oz (180 mL) bottles Total - 12 fl oz (360 mL), For Ages 12+, Dist. by Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC 63824-528-22-01, NDC 63824-528-22-00, UPC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1360-2015·2015-09-02
Bactroban Ointment Recalled for Penicillin Contamination and Foreign Substances
GlaxoSmithKline is recalling Bactroban Ointment due to penicillin cross-contamination and foreign substances found during manufacturing.
Product
Bactroban Ointment (mupirocin calcium), 2% 22g tube ,Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217. NDC 0029-1525-44
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1362-2015·2015-09-02
GlaxoSmithKline Recalls Mupirocin Calcium Cream Due to Penicillin Contamination
GlaxoSmithKline is recalling Mupirocin Calcium Cream, 2%, because the product was contaminated with penicillin and foreign substances during manufacturing.
Product
Mupirocin Calcium Cream, 2%, a) 15g tube (NDC 66993-942-15),b) 30g tube (NDC 66993-942-31), Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1355-2015·2015-09-02
PharMEDium Recalls Heparin Sodium Injection Bags Due to Particulate Matter
PharMEDium Services is recalling 480 bags of Heparin Sodium Injection USP due to the presence of particulate matter. The product was distributed nationwide.
Product
HEPARIN Sodium Injection USP, 12,500 USP Units added to 250 mL 5% Dextrose Injection USP (50 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0418, NDC# 61553-418-02.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V552000·2015-09-02
Forest River Recalls 2016 Shasta Airflyte Trailers Due to Tire Clearance Defect
Forest River is recalling 2016 Shasta Airflyte 16 and 19 trailers because insufficient tire clearance may cause tire failure and increase crash risk.
Product
SHASTA — SHASTA AIRFLYTE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1353-2015·2015-09-02
Pharmedium Recalls Oxytocin Injection Bags Due to Particulate Matter
Pharmedium Services, LLC is recalling 72 bags of oxyTOCIN 15 Units in 5% Dextrose Injection due to the presence of particulate matter.
Product
oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP, packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K2677, NDC# 61553-777-02.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V551000·2015-09-02
Foretravel Recalls 2012-2014 Motorhomes Due to Loose Front Ball Joints
Foretravel is recalling 2012-2014 Nimbus, Phenix, and IH45 motorhomes because loose front ball joints may separate, causing loss of steering control and increasing crash risk.
Product
FORETRAVEL — FORETRAVEL NIMBUS, IH45, PHENIX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-3048-2015·2015-09-02
Veggie Evolution Kale Crisps Recalled for Undeclared Soy
It Takes A Village Foods is recalling Veggie Evolution Kale Crisps Zen Nori because the product contains soy, which is not declared on the label.
Product
Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly pouch has a net weight 1.5 oz. There are six packages per case. UPC is 7 13757 57480 8. The product's label is read in part: "***VEGGIE EVOLUTION***KALE…
Category
Food
Distribution
22 states
SevereFDA (Devices)·Z-2451-2015·2015-09-02
Synthes Trauma Ex-Fix System Recalled for MR Labeling Corrections
Synthes (USA) Products LLC is recalling the Trauma Ex-Fix System to correct MRI safety labeling. The recall identifies additional part numbers as MR Conditional and notes one serious injury.
Product
Synthes Trauma Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended to stabilize and provide treatment for fractures of the small bones, such as the hand, wrist, forearm, foot, and ankle; (M) for the construction of an external fixation frame for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2462-2015·2015-09-02
Arrow International Recalls PICC Kits with Potential Peel-Away Sheath Defect
Arrow International is recalling 52,109 PICC kits because the peel-away sheath hub tabs may prematurely detach. One injury has been reported.
Product
PICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic, ultrasound Product Usage: catheter, intravascular, therapeutic, ultrasound
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2456-2015·2015-09-02
Trilliant Surgical Reamer Heads Recalled for Guide Pin Fit Issues
Trilliant Surgical Ltd. is recalling 638 Concave and Convex Reamer Heads because the cannulation may be too small to allow the Guide Pin to pass through freely.
Product
Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, 20 mm; Concave Reamer Head 22 mm; Convex Reamer Head, 16 mm; Convex Reamer Head, 18 mm; Convex Reamer Head 20 mm; Convex Reamer Head 22 mm, used with Gridlock Plating system, for use in trauma and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2440-2015·2015-09-02
Brainlab ExacTrac 6.0 Patient Positioning System Recalled for Display Error
Brainlab AG is recalling ExacTrac 6.0.x software due to a potential display error in Digitally Reconstructed Radiographs used for x-ray correction.
Product
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures.
Category
Medical Device
Distribution
32 states