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. 1,920 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,920 in last 12 months

Showing 2352123540 of 29,737 recalls

Medical DeviceApril 16, 2015· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon Oval MRI System Recalled by Hitachi Medical Systems America...

The Issue: Image data transferred from the MRI system to a workstation showed errors on...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...

The Issue: Image data transferred from the MRI system to a workstation showed errors on...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Nihon Kohden America Inc

Recalled Item: Remote Network Station Recalled by Nihon Kohden America Inc Due to Nihon...

The Issue: Nihon Kohden America (NKA) is recalling the Remote Network Station (RNS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Halyard Health, Inc

Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the cable cart and the corrugated hose are unable to move freely, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Drum Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH -4MM Carbide Fluted Ball Recalled by The Anspach Effort, Inc. Due to...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 8MM x 14MM Fluted Drum Recalled by The Anspach Effort, Inc. Due to...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 5MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 2.3MM Fluted Matchstick Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 4MM x 11 MM Fluted Barrel Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· CooperSurgical, Inc.

Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...

The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Extra Coarse Diamond Ball Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing