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. 1,748 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,748 in last 12 months

Showing 4684146860 of 54,363 recalls

DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· McKesson Packaging Services

Recalled Item: Venlafaxine Hydrochloride Recalled by McKesson Packaging Services Due to...

The Issue: Failed Dissolution Specification: Out of Specification dissolution results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
FoodFebruary 28, 2014· Unilever United States, Inc.

Recalled Item: Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs...

The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 28, 2014· Mars Food US

Recalled Item: UNCLE BEN's(R) READY RICE(R) Original Enriched Long Grain White Rice...

The Issue: Voluntary recall was initiated after identifying a number of packages with...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 28, 2014· High Mowing Organic Seed

Recalled Item: High Mowing Organic Sprouting Seeds Ancient Eastern Blend Recalled by High...

The Issue: Contains undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...

The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Teleflex Medical

Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...

The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...

The Issue: GE Healthcare has recently become aware of potential safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing