Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,573 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,573 in last 12 months

Showing 23212340 of 27,512 recalls

Medical DeviceDecember 20, 2024· Max Mobility LLC

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.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Max Mobility LLC

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.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Ethicon, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750 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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Boston Scientific Corporation

Recalled Item: 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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Continu-Flo Solution Set with Duo-Vent Spike Recalled by Baxter...

The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing