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. 1,744 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,744 in last 12 months

Showing 5138151400 of 54,363 recalls

FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Marine Lobster Spread (8oz and 16oz in flexible Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Smoked Salmon Spread (8oz and 16oz in flexible Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Lobster & Shrimp Spread (8oz and 16oz in Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Blue Crab Spread (8oz and 16oz in flexible Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
DrugFebruary 1, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: CALCIUM GLUCONATE INJECTION Recalled by Fresenius Kabi USA LLC (FK USA) Due...

The Issue: Labeling: Missing label

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

Class III — Low RiskOngoing
Refund
DrugFebruary 1, 2013· Ferring Pharmaceuticals Inc

Recalled Item: TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Recalled...

The Issue: Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax (cefixime for oral suspension) USP Recalled by Lupin Pharmaceuticals...

The Issue: Discoloration; Product may not meet specifications for color description...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2013· Gilead Sciences, Inc.

Recalled Item: Vistide (cidofovir) Injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter was found in some vials...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 31, 2013· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus...

The Issue: During the course of product monitoring, Siemens became aware of a tolerance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2013· Medtronic Navigation, Inc.

Recalled Item: Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic...

The Issue: Potential failure of the braking system that controls the O-arm Imaging...

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

Class II — Potential Health HazardOngoing