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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.
Showing 1641–1660 of 49,976 recalls
Recalled Item: Philips CT systems labeled as the following: 1. Big Bore RT Recalled by...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. CT 6000 Recalled by Philips...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance 16 Power Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT 728326 Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity Core128 Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT SP Recalled...
The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 900 COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 690T COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 COULTER Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Hematology analyzers configured with HGB photometers may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tavaborole Topical Solution 5% Recalled by VIONA PHARMACEUTICALS INC Due to...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...
The Issue: Limited system movements after startup .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to...
The Issue: Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.