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. 2,370 recalls have been distributed to Kansas in the last 12 months.
Showing 41721–41740 of 50,117 recalls
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by...
The Issue: The firm is distributing the Rejuvenator device without an approved 510(k).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is...
The Issue: CareFusion has identified a potential for damage to the power connector on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5%...
The Issue: Presence of Particulate Matter: particulate matter was found during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PERSONA" The Personalized Knee System UC Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...
The Issue: Reports of unexpected movement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...
The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...
The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.