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. 1,893 recalls have been distributed to Kansas in the last 12 months.
Showing 18461–18480 of 28,538 recalls
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 5 Fr. Peripherally Recalled by Arrow...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit. The MAC Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickFlash Radial Artery/Arterial Line Catheterization Kit The Arrow¿...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High...
The Issue: The large-bore two-lumen catheter permits venous access to the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-Lumen Hemodialysis Catheterization Kit with Blue Flex Tip(R) Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable PICC Kit The Arrow International Pressure...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology...
The Issue: When the Smart Check tool is used to perform a Smart Setup with one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit. The large-bore...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R)...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology A PICC permits venous access Recalled...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIZA Vertebral Body Replacement Recalled by Eden Spine Europe SA Due to...
The Issue: Complaints that implants have been disassembled by surgeons because of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Estradiol II Recalled by BioMerieux SA Due to Fulvestrant cross reacts...
The Issue: Fulvestrant cross reacts with the VIDAS Estradiol II immunoassay and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ Administration Set Recalled by Smiths Medical ASD Inc. Due to Smiths...
The Issue: Smiths Medical has become aware that the drawing on the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation Recalled...
The Issue: Medtronic received reports that the DBS depth stop did not adequately secure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Operation Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cataract Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.