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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 18941–18960 of 49,976 recalls
Recalled Item: Dermatone (avobenzone Recalled by Filltech USA, LLC Due to Microbial...
The Issue: Microbial contamination of non-sterile products: positive test for yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermatone (avobenzone Recalled by Filltech USA, LLC Due to Microbial...
The Issue: Microbial contamination of non-sterile products: positive test for yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: SubPotent Drug: Low out-of-specification results for assay testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc. Due to CGMP...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine Hydrochloride Capsules Recalled by Aurobindo Pharma USA Inc. Due...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Tablets USP 750 mg 120-count bottles Recalled by Aurobindo...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Aurobindo Pharma USA Inc....
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to CGMP...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Aurobindo Pharma USA Inc. Due to CGMP...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.