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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.
Showing 14381–14400 of 49,976 recalls
Recalled Item: Chocolate & the Chip The Funfetti Cookie Cake Cookie cakes: Recalled by...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Octoberfest Cookies: 4 oz / 114 Recalled by Chocolate...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Gluten Free Nutella cookie Cake: Cookie Recalled by...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Maple Macadamia Cookies: 4 oz / Recalled by Chocolate...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Brown Butter Rice Crispy Treat - Recalled by Chocolate...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Almond Flour Crackers fine ground sea salt packaged in a Recalled by SIMPLE...
The Issue: Undeclared Milk Allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Boozy Banana Walnut: Cookies: 4 oz Recalled by...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications and Presence of Foreign Tablets/Capsules;...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: CGMP Deviations: Customer complaint for the presence of a staple co-mingled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betaxolol Ophthalmic Solution Recalled by Akorn, Inc. Due to Microbial...
The Issue: Microbial Contamination of Sterile Products: Confirmed sterility failure...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cliquid MD version 3.4 software used in conjunction with Analyst Recalled by...
The Issue: The values of the Internal Standard (IS) concentrations are incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE...
The Issue: Due to component (housing and plunger) detaching from the semi-automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 6x120 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.010 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 6x150 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.