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. 2,664 recalls have been distributed to Oklahoma in the last 12 months.
Showing 4041–4060 of 13,376 recalls
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: 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: 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: 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: 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: 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: 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: 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 Eucalyptus Mint Sanitizing Handwash (Benzalkonium Chloride...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...
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: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...
The Issue: CGMP Deviaitons
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...
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: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Moisture Limits: Out of specification for water content
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC 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: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...
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: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 200 units/mL (U-200) Recalled...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.