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. 1,160 recalls have been distributed to Kansas in the last 12 months.
Showing 281–300 of 50,117 recalls
Recalled Item: Medline Convenience Kits: 1) LITHOTOMY PACK Recalled by Medline Industries,...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) KIT UROLOGY SLING Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) ADMIT KIT Recalled by Medline Industries, LP...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) SCC RF PAIN MGMT Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS Recalled by Medline...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) PICC LINE TRAY Recalled by Medline Industries,...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits: 1) HYSTEROSCOPY Recalled by Medline Industries, LP...
The Issue: Medline has identified issues related to calibration of the equipment used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...
The Issue: Devices which did not undergo thermoforming could deform and lose performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQ 120 GFEW Recalled by Encon Safety Products Co Due to cGMP deviations.
The Issue: cGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...
The Issue: The mix up of the impression caps provided in the package. The provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HerbsForever- Hingwastika Churna Recalled by Herbs Forever Due to Undeclared...
The Issue: Potential undeclared allergen ingredient (Wheat)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HerbsForever- Gastro Care Recalled by Herbs Forever Due to Undeclared Allergen
The Issue: Potential undeclared allergen ingredient (Wheat)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...
The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.