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. 2,580 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15841–15860 of 49,976 recalls
Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...
The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...
The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Krazy Night capsule Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shogun-X capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs up 7 Red 70K capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triple SupremeZen Gold 3500 Recalled by Na Na Collection Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Platinum 5000 Recalled by Na Na Collection Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...
The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnia Soft Tissue Punch is a dental instrument designed to Recalled by Omnia...
The Issue: Omnia SRL received a notification from the contract manufacturer informing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shogun-X 7000 capsule Recalled by Nuri Trading LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs Up 7 White 11K capsule Recalled by Nuri Trading LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs Up 7 Black 25K capsule Recalled by Nuri Trading LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 69MODE Blue 69 capsule Recalled by Nuri Trading LLC Due to Undeclared Tadalafil
The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Stability Specifications: product did not meet viscosity results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: foamyiQ Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%) Recalled...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy E2 Sanitizing Handwash (Benzalkonium Chloride Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antiseptic Hand Cleaner (Chloroxylenol Recalled by Spartan Chemical Co Inc...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%)...
The Issue: Microbial Contamination of Non-Sterile Products; lot tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite'n Foamy Eucalyptus Mint Sanitizing Handwash (Benzalkonium Chloride...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.