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. 2,420 recalls have been distributed to Kansas in the last 12 months.
Showing 31261–31280 of 50,117 recalls
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast sodium tablets Recalled by Hetero USA Inc Due to Discoloration:...
The Issue: Discoloration: the firm received a complaint of a sealed bottle in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) VANTA¿ XRF...
The Issue: It was discovered under rare circumstances the LED warning light circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller...
The Issue: The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color contact lenses labeled under the following brands: Diamond Recalled by...
The Issue: Sterility and Misbranding: Lenses may not be sterile and may be labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System - C-Spine Coil Recalled by Hitachi Medical Systems...
The Issue: The customer indicated that the coil balun was hot to the touch when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Presence of Foreign Substance: consumer complaint for foreign matter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...
The Issue: There is a possibility for data to be stored under the wrong patient on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: The company received a customer complaint for the inability to calibrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cappuccino Snack Mix Lot code: 20161027 Recalled by Dutch Valley Food...
The Issue: As a result of an ingredient supplier recall, Dutch Valley is issuing a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI Progesterone Recalled by Siemens Healthcare...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: DHEA-S causes falsely elevated progesterone results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...
The Issue: packaging of some femoral components was incorrectly labeled as either...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.