Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,553 recalls have been distributed to Oklahoma in the last 12 months.
Showing 19201–19220 of 49,976 recalls
Recalled Item: Natural Grocers Organic Extra Virgin Coconut Oil Recalled by Vitamin Cottage...
The Issue: Product tested high for mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Natural Grocers Organic Extra Virgin Coconut Oil Recalled by Vitamin Cottage...
The Issue: Product tested high for mold.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...
The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...
The Issue: The firm has received an increased number of complaints concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...
The Issue: Defective Container: products potentially could have been packaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...
The Issue: Defective Container: products potentially could have been packaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Programmer Recalled by LivaNova USA Inc Due to False positive...
The Issue: False positive warning may occur after: 1) VNS Generator interrogated at 0mA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris PCA Module Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Pump Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Extra Strength Acetaminophen Tablets Recalled by Contract Pharmacal...
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Extra Strength Acetaminophen Tablets Recalled by Contract Pharmacal...
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by Pfizer Inc. Due to Defective Container:...
The Issue: Defective Container: confirmed customer reports for vials with loose metal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ABL90 FLEX PLUS Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.