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. 981 recalls have been distributed to Oklahoma in the last 12 months.
Showing 38141–38160 of 49,976 recalls
Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril maleate and hydrochlorothiazide tablets USP Recalled by Apotex...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PowerLED / X-TEN / VOLISTA Surgical Light Systems are Recalled by Maquet...
The Issue: Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 3131IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 540. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 620. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA DX-D 100 is a mobile digital radiography x-ray system Recalled by AGFA...
The Issue: When using the DX-D 100 unit, sporadic unintended movements caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.