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. 1,128 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,128 in last 12 months

Showing 2521–2540 of 54,363 recalls

Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Upgrade to MR 7700 Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 3.0T Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T S Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Elition X Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for XR and 3.0T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for 1.5T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Ambition S Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Elition S Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for 3.0T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Ambition X Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to Ingenia Elition X Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Evolution Upgrade 1.5T Recalled by Philips North America Llc...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· Fresenius Kabi USA, LLC

Recalled Item: IVENIX INFUSION SYSTEM LVP Blood Products Administration Set Recalled by...

The Issue: Mis-assembly error of Blood Products Administrations Sets where the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Matcha Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Brown Sugar Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Taro Flavor Recalled by R&M TRADING LLC Due to The Instant...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Original Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Honeydew Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund