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. 1,059 recalls have been distributed to Kansas in the last 12 months.
Showing 14301–14320 of 28,538 recalls
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 15 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System 10 MM Recalled by Conmed Corporation...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmable Pump Recalled by Flowonix Medical Inc Due to The pump...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Clinician Programmer (Touchscreen) Software version 2.00.29...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra Programmer (Grand Prime) Software version 2.00.29 Recalled by...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump Recalled by Flowonix Medical Inc Due to The...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump (Clinical) Recalled by Flowonix Medical Inc...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Low Base Recalled by Community Products, LLC Due to A design...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Standard Base Recalled by Community Products, LLC Due to A...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: Potential for sample fluid to be dispensed to an incorrect position on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON...
The Issue: Advisory issued not to disable or bypass the AMP function. Disabling or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...
The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performance Series Sagittal Blade Recalled by Stryker Instruments Div. of...
The Issue: During manufacture, packaging materials for a small portion of the lot may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due...
The Issue: When the user performs the re-assignment of a parent / companion pair, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIR Technology Anterior Array Recalled by GE Healthcare, LLC Due to The...
The Issue: The outer seam of the coil, closest to the system cable, may separate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neomem Resorbable Collagen Membrane Recalled by Collagen Matrix, Inc. Due to...
The Issue: Product was packaged in the wrong box; may have been placed inside a Neomem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.