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. 2,576 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16221–16240 of 49,976 recalls
Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...
The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylprednisolone Tablets USP Recalled by Jubilant Cadista Pharmaceuticals,...
The Issue: Labeling: Illegible label: Customer complaint received of mis-alignment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01...
The Issue: Crystallization: customer complaints for crystallization in finished product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01...
The Issue: Crystallization: customer complaints for crystallization in finished product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ferrara Candy Company assorted candy Heart Box Recalled by Ferrara Candy...
The Issue: Undeclared ingredients on retail packaging, including but not limited to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...
The Issue: The product may be contaminated with Burkholderia cepacia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...
The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...
The Issue: Teleflex is voluntarily recalling the products above due to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methacholine Challenge 5-Syringe Test Kits Recalled by Edge Pharma, LLC Due...
The Issue: Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 100mg Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...
The Issue: Discoloration and turbidity were present in the specified lots of STMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...
The Issue: Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.