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. 1,893 recalls have been distributed to Kansas in the last 12 months.
Showing 19741–19760 of 28,538 recalls
Recalled Item: Bifurcated SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triple Line SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir and 2 Recalled...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir Recalled by...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Reservoir and 2 Blood Sampling...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TP4 Kit with 10cc SafeSet Reservoir Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Kit with SafeSet and 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Cable. Part Numbers: 4460 Recalled by Blackrock Microsystems, LLC...
The Issue: Blackrock Microsystems, LLC announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neural Signal Amplifier. Part Numbers: 4208 Recalled by Blackrock...
The Issue: Blackrock Microsystems, LLC announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Monitoring Kit with SafeSet Reservoir and Blood Sampling Port...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Blood Sampling Ports Recalled by...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc. Due to...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitoring Kit with 03mL Flush Device Recalled by ICU Medical, Inc. Due to...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitoring Kit with TP4 Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 Recalled by Mentor...
The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Recalled by...
The Issue: Contents of the package do not match the product labeling. Product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Targeting Arm Guide Recalled by Zimmer Biomet, Inc. Due to Old...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Soft Tissue Sleeve Guide Recalled by Zimmer Biomet, Inc. Due...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.