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. 2,616 recalls have been distributed to Kansas in the last 12 months.
Showing 4941–4960 of 50,117 recalls
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft Infusion Set Recalled by Unomedical A/S Due to Specific VariSoftTM...
The Issue: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ClotTriever XL Catheter Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy system catheter instructions for use updated to reduce adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective container; yellow colored spike from cap lodged in the nozzle
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Umary Acido Hialuronico Recalled by MAIN PRODUCTS INC Due to Undeclared...
The Issue: Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...
The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...
The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for Recalled by...
The Issue: May intermittently produce falsely resistant results for pyrazinamide (PZA)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...
The Issue: Software anomalies which can result in two separate issues: A lagging screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Temperature Controlled Recalled by Beckman Coulter Biomedical...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.