Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,004 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,004 in last 12 months

Showing 31721–31740 of 54,363 recalls

Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing Recalled by ConvaTec, Inc...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Masks Recalled by ConvaTec, Inc Due to Reports of tubing detaching...

The Issue: Reports of tubing detaching from oxygen masks either prior to use (in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreathing Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· Medtronic Navigation, Inc.

Recalled Item: Install CD Recalled by Medtronic Navigation, Inc. Due to Software issue...

The Issue: Software issue related to the StealthStation S7 system and the Synergy Spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Masks Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
DrugMay 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Introducer Kit with Integral Hemostasis Valve/Side Port Recalled by Arrow...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended Recalled by...

The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to Incorrect labeling; the box...

The Issue: Incorrect labeling; the box label indicates Pediatric, the product insert...

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

Class II — Potential Health HazardOngoing