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. 2,603 recalls have been distributed to Kansas in the last 12 months.
Showing 6721–6740 of 50,117 recalls
Recalled Item: TrueDent Cyan Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Magenta Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent White Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS5HND / Integra Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP04 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7260 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : 31156 / COMBO KIT CONTAINS INS-8301 Recalled by Integra LifeSciences Corp....
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHND / Integra¿ Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHRZN / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...
The Issue: Devices without transmural drainage holes may be mislabeled as devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Woodstock 5 Grain Cereal. Oats Recalled by UNFI General Corporate Due to The...
The Issue: The ingredient Triticale is not identified as wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Glimepiride Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Misprint on tablet
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glimepiride Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Misprint on tablet
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lurasidone Hydrochloride Tablets 60mg Recalled by SUN PHARMACEUTICAL...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zolpidem Tartrate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.