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. 1,039 recalls have been distributed to Kansas in the last 12 months.
Showing 17381–17400 of 50,117 recalls
Recalled Item: GORE TAG CONFORMABLE Thoracic Stent Graft with ACTIVE CONTROL System...
The Issue: Due to secondary deployment fiber being attached to secondary deployment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA FAST-FIX AB ASSEMBLY-REVERSE CURVE-Absorbable Suture anchor Product...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 W/ 1 UB COBRAID BLACK-Absorbable Suture anchor Product...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 W. UB COBRAID BLUE-Absorbable Suture anchor Product Number:...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR-Absorbable Suture anchors Product Number:...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR WITH TWO- Absorbable Suture anchors Recalled...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BL-- Recalled by Smith & Nephew, Inc....
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Failed Impurities/Degradation Specifications; high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...
The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...
The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L22mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 28-33mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 33-42mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 42-58mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L24mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.