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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.
Showing 21941–21960 of 49,976 recalls
Recalled Item: Lidocaine 0.5%/Phenylephrine 0.75% P.F. INJ Recalled by Premier Pharmacy...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Preservative Free Sterile Solution for INJ...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isoproterenol HCL in D5W (Sterile to Sterile) Recalled by Premier Pharmacy...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Naloxone HCL Preserved INJ Recalled by Premier Pharmacy Labs Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orphenadrine Citrate Sterile Injectable Solution *Contains Sulfites*...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Riboflavin 5-Phosphate Sodium Ophthalmic Solution Recalled by Premier...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mitomycin Preservative Free Irrigation Recalled by Premier Pharmacy Labs Inc...
The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Recalled by...
The Issue: Elevated levels of inorganic arsenic
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...
The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...
The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depth Electrodes Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versa - Kath Mini Kit Recalled by Epimed International, Inc. Due to Mislabeling
The Issue: Mislabeled - The product's labeling contains an incorrect size for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versa - Kath Mini Kit Recalled by Epimed International, Inc. Due to Mislabeling
The Issue: Mislabeled - The product's labeling contains an incorrect size for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal THE RESOURCE GROUP Recalled by DeRoyal Industries Inc Due to Custom...
The Issue: Custom surgical packs are being recalled because it contains Cardinal Health...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...
The Issue: The products' cut, coagulate, or blend function may not operate with the use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices may indicate that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...
The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.