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. 2,379 recalls have been distributed to Oklahoma in the last 12 months.
Showing 46941–46960 of 49,976 recalls
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntellVue Info Center iX 866023 Recalled by Philips Healthcare Inc....
The Issue: If a customer creates customized trend scales in the trend review tile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20-Pole Eco Cable Recalled by Biosense Webster, Inc. Due to Biosense is...
The Issue: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chicken of the Sea 5-Ounce Chunk Light Tuna in Oil. Recalled by Tri-Union...
The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chicken of the Sea Brand 5-ounce chunk white albacore tuna Recalled by...
The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Siemens syngo.plaza SW version VA20 with Mammography license. image...
The Issue: Siemens issued a Customer Safety Notice to inform customers of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect QLC1677E Recalled by Steris Corporation Due to During a...
The Issue: During a routine label review, the firm identified four SYSTEM 1E Quick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz Dual series CT Scanner System Recalled by Philips And Neusoft Medical...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse...
The Issue: The product specifications sheet, part of the Instructions for Use (IFU),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...
The Issue: An internal review of CareFusion's labeling for preoperative skin prep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.