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. 2,636 recalls have been distributed to Kansas in the last 12 months.
Showing 2561–2580 of 50,117 recalls
Recalled Item: ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug Group LLC...
The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " Recalled by Prismatik...
The Issue: Due to packaging mix up. Package of finished devices were reported to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges...
The Issue: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus Initial Drill Recalled by Straumann USA LLC Due to The batch was...
The Issue: The batch was produced without the laser engraving of 7 mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin...
The Issue: The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled:...
The Issue: Contains undeclared allergens (almonds).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Recalled by Medical...
The Issue: Potential for DC Power Supply housing to become hot to the touch and deform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Occlusion Catheter. Catalog Numbers: 2103-36 Recalled by LeMaitre...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X)...
The Issue: Potential for the presence of visible foreign matter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09 Recalled by...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Craniotomy Kit Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator Recalled by Integra LifeSciences Corp....
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE hydrochloride Capsules USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: an out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Eugia US LLC Due to cGMP:...
The Issue: cGMP: complaints of crystals not redissolving into solution after warming...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355 Recalled...
The Issue: Field action to clarify the flow rates and inlet fluid temperatures, along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.