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. 2,638 recalls have been distributed to Oklahoma in the last 12 months.
Showing 9881–9900 of 49,976 recalls
Recalled Item: Nose Better Gel (0.75% Camphor Recalled by Ecometics, Inc. Due to CGMP...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 1 Recalled by SCA Pharmaceuticals Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...
The Issue: Problem maintaining the stable placement of the battery may come loose from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iradimed Corporation MRidium MRI 1000 Series Infusion Sets Recalled by...
The Issue: Certain Iradimed 1057 Syringe Adapter Sets, used with the MRidium MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clear Eyes Recalled by Teva Pharmaceuticals USA Inc Due to Failed Impurities...
The Issue: Failed Impurities Specification: Out-of-specification (OOS) stability test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NaturalCare bioAllers Recalled by Nutraceutical Corporation Due to CGMP...
The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NaturalCare bioAllers Recalled by Nutraceutical Corporation Due to CGMP...
The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NatraBio Recalled by Nutraceutical Corporation Due to CGMP Deviations: Raw...
The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NaturalCare Recalled by Nutraceutical Corporation Due to CGMP Deviations:...
The Issue: CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets Recalled by The Harvard Drug Group Due to...
The Issue: Packaging defect: observed packaging defect, blister packaging inadequately...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and Recalled by...
The Issue: Mislabeled: Product is marked with GTIN # 04046955299592 however; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...
The Issue: There have been complaints that the clip did not come out of the tube sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor is a portable vital signs monitor Recalled by...
The Issue: During internal testing, Regulatory Compliance issues were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl in 0.9% Sodium Chloride Injection Recalled by Nephron...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl in 0.7% Sodium Chloride Injection Recalled by Nephron Sterile...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.