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. 2,636 recalls have been distributed to Kansas in the last 12 months.
Showing 2341–2360 of 28,538 recalls
Recalled Item: MEDLINE ARTERIAL LINE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Certain lots Sterile Infusion Catheters which were mislabeled as having a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTURION Infusion Catheter Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Certain lots Sterile Infusion Catheters which were mislabeled as having a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...
The Issue: Due to internal venturi component getting transiently stuck in the forward...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE Polypropylene Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL Polyester Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERMA-HAND Silk Suture Recalled by Ethicon, LLC Due to Sutures may have an...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740 Recalled by Boston...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.