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. 1,099 recalls have been distributed to Kansas in the last 12 months.
Showing 5561–5580 of 50,117 recalls
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets Recalled by Glenmark...
The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Golden State Medical Supply...
The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets Recalled by Glenmark...
The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vasopressin Injection Recalled by American Regent, Inc. Due to Subpotent...
The Issue: Subpotent product in addition to having out-of-specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sight OLO CBC Test Kit Recalled by SIGHT DIAGNOSTICS LTD Due to One Test Kit...
The Issue: One Test Kit lot (TK1-10114) shows a positive bias in the platelet count due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in...
The Issue: The reason for recall is the meters may show an incorrect measurement unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...
The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeos Robotic Digital Microscope Recalled by Aesculap Inc Due to Possibility...
The Issue: Possibility of the robotic arm to drop more than 10cm from its original...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring System Recalled by Draeger...
The Issue: Device is not in full compliance to Type CF requirements of IEC 60601-1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...
The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Darby Prophylaxis Paste with 1.23% Fluoride Ion Recalled by Young Dental...
The Issue: Part number 040032, Lot number, 248607 was incorrectly labeled as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile Recalled by SVS LLC Due to Mislabeling
The Issue: Firm received complaints regarding skin irritation when using the gloves,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...
The Issue: The wrong configuration of the blade was in the package. The bevel was on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II (polydioxanone) Suture - Intended for use in general Recalled by...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL (polyglactin 910) Suture - Indicated for use in general Recalled by...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in Recalled...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica HistoCore Arcadia H Recalled by LEICA BIOSYSTEMS NUSSLOCH GMBH Due to...
The Issue: An issue with safe usage of the device was identified whereby toxic smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONOCRYL (poliglecaprone 25) Suture - Intended for use in general Recalled...
The Issue: Issue on a specific packaging machine resulted in a hole in the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...
The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI systems: Vantage Orian MRT-1550 (MEXL-1550) Recalled by Canon Medical...
The Issue: The terminal block used to secure the power supply cable for the gradient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.