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. 1,913 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,913 in last 12 months

Showing 2456124580 of 29,737 recalls

Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Alliance Tech Medical, Inc

Recalled Item: Alliance Tech Medical Recalled by Alliance Tech Medical, Inc Due to Patients...

The Issue: Patients have experienced a bad taste associated with the filters.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Monteris Medical Corp

Recalled Item: SideFire Directional Laser Probe Recalled by Monteris Medical Corp Due to...

The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Monteris Medical Corp

Recalled Item: FullFire Diffusing Tip Laser Probe Recalled by Monteris Medical Corp Due to...

The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2014· Zimmer, Inc.

Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...

The Issue: Failed to meet established requirements for sterile barrier integrity due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes Radiolucent Retractor Recalled by Synthes, Inc. Due to...

The Issue: Particle residue on the instrument from adhesive tape which was used to bind...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...

The Issue: A software issue may lead to ventilator inoperative situations.

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer, Inc.

Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...

The Issue: The affected products are missing polar boss threads.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Medartis, Inc.

Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...

The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Roscoe Medical Inc

Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...

The Issue: The caster may separate completely from the device frame causing injury to user.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· IMRIS Inc

Recalled Item: IMRIS Operating Room table (ORT200 and ORT300). Intended for use Recalled by...

The Issue: One of the three pins that is used to hold the ORT200 table alignment block...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...

The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: Certain lots of the reagent cartridges show confirmed positive bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2014· Signal Medical Corporation

Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...

The Issue: Packaging of a device was compromised

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

Class II — Potential Health HazardOngoing