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. 1,854 recalls have been distributed to Kansas in the last 12 months.
Showing 25001–25020 of 28,538 recalls
Recalled Item: Smith & Nephew RENASYS Soft Port (The RENASYS Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...
The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...
The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panaroma Central Station Product Usage: This device can view real time...
The Issue: Mindray has identified two issues with the Panorama Central Station. Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...
The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular...
The Issue: Defective component may cause extension sets to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...
The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...
The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infantino Squeeze & Teethe Monkey Recalled by Infantino LLC Due to Infantino...
The Issue: Infantino initiated this voluntary recall of all lots of Infantino Squeeze &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 Recalled by...
The Issue: Complaints were received regarding Quality Control (QC) shifts with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atlantis PV Recalled by Boston Scientific Corporation Due to Reports of...
The Issue: Reports of physicians experiencing inability to pass a 0.035" guidewire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...
The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.