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. 2,566 recalls have been distributed to Kansas in the last 12 months.
Showing 12061–12080 of 28,538 recalls
Recalled Item: Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xience Sierra TM Everolimus Eluting Coronary Stent System Recalled by Abbott...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. Braun Introcan Safety IV Catheters Recalled by Janus Trade Group Due to...
The Issue: Distribution of B.Braun Introcan Safety IV catheters without a 510(k) within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is Recalled...
The Issue: It was identified that there is a potential for the Stim Interconnecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for...
The Issue: It was identified that there is a potential for the Stim Interconnecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...
The Issue: There was no data to validate that the identified endo-therapy devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...
The Issue: There was no data to validate that the identified endo-therapy devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre 5F Plus Over the Wire Embolectomy Catheter Recalled by LeMaitre...
The Issue: There has been an increased trend in reports of catheters failing to deflate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Utak NR Trace Elements Serum Control Recalled by Utak Laboratories Inc Due...
The Issue: The product has an incorrect value for cadmium and an incorrect expected range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifePAK 500 Automated External Defibrillator Recalled by Physio-Control,...
The Issue: Automated External Defibrillators may not detect a patient connection due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.