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. 2,458 recalls have been distributed to Oklahoma in the last 12 months.
Showing 34081–34100 of 49,976 recalls
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...
The Issue: Defective Delivery System: Defective stem valve causes leakage of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...
The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Recalled by...
The Issue: Due to the buildup of grease within the hose and motor, the product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norditropin FlexPro Somatropin (rDNA origin) injection Recalled by Novo...
The Issue: Defective Delivery System; may have a low frequency assembly fault which may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection Recalled by Teva North America Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Due to potential for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...
The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Microline Scissor Tips intended to be used with a Recalled by...
The Issue: Sterlilmed is recalling all unexpired Scissor Tips because of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT-S(64) 4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The bracket that is used to lift the cover has bolts that were not welded in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: The bracket that is used to lift the cover has bolts that were not welded in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: The bracket that is used to lift the cover has bolts that were not welded in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5 Recalled by Volcano Corporation Due to Volcano has become aware...
The Issue: Volcano has become aware of an incompatibility issue between Impacted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT S(20) - 4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: The bracket that is used to lift the cover has bolts that were not welded in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breathe Right Clear Recalled by GSK Consumer Healthcare Due to Some cartons...
The Issue: Some cartons used in the secondary packaging of Breathe Right Clear, Large,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensorcaine- MPF (Bupivacaine HCI Injection Recalled by Fresenius Kabi USA,...
The Issue: Presence of Particulate Matter: Glass particulate found in sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Winn Dixie 32 oz. Sock It To Me Creme Cake Recalled by Benson's Old Home...
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Winn Dixie 14 oz. Sliced Vanilla Cream Cake Recalled by Benson's Old Home...
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.