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. 2,785 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,785 in last 12 months

Showing 998110000 of 54,363 recalls

Medical DeviceApril 21, 2023· Masimo Corporation

Recalled Item: Masimo LNOP TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...

The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.

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

Class II — Potential Health HazardOngoing
FoodApril 20, 2023· Euro-Pharma

Recalled Item: Multiple Vitamin B Capsules Recalled by Euro-Pharma Due to Undeclared Allergen

The Issue: undeclared allergen (milk)

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2023· Bryant Ranch Prepack, Inc.

Recalled Item: Lidocaine Patch 5% Recalled by Bryant Ranch Prepack, Inc. Due to Labeling:...

The Issue: Labeling: Typographical error on the upper left-hand side of the box and...

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

Class III — Low RiskOngoing
Refund
DrugApril 19, 2023· Sun Pharmaceutical Industries Ltd.

Recalled Item: Fyremadel (ganirelix acetate) injection Recalled by Sun Pharmaceutical...

The Issue: Presence of Particulate Matter: A piece of glass was found in a prefilled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2023· Philips North America

Recalled Item: Patient Information Center iX Recalled by Philips North America Due to...

The Issue: During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Single Use Distal Cover Model Number MAJ-2315 used with Recalled by...

The Issue: The Single Use Distal Cover MAJ-2315 may cause mucosal injury and/or become...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: ID Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax 1 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Set2Go Ventilation 12 (A) Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax HEPA Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Seattle PAP Plus Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia WT (P)180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Set Coax 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist catheter is an intravascular micro axial...

The Issue: The Impella 5.5 pump experienced a heightened complaint rate for purge leaks.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· DeRoyal Industries Inc

Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...

The Issue: The custom procedure packs contain light handle covers that have been...

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

Class II — Potential Health HazardOngoing