Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,059 recalls have been distributed to Kansas in the last 12 months.
Showing 15801–15820 of 50,117 recalls
Recalled Item: Tuscan Garden Ranch Dressing Recalled by Richelieu Foods, Inc. Due to An...
The Issue: An incorrect label was applied to the back of ranch dressing bottles. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...
The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...
The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...
The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...
The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...
Recommended Action: Stop using. Contact the manufacturer or your 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: 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: 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: 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: 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: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas Liat Analyzer: respiratory virus panel nucleic acid assay system...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B assay cobas Liat- Reagents Recalled by...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Model Number: (9A)9.0.0.113 Recalled by RAYSEARCH LABORATORIES AB...
The Issue: Flags edited in RayCare after a patient has been checked in may not always...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Biopsy Device Recalled by Zavation Due to Products distributed as...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.