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. 1,825 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,825 in last 12 months

Showing 3670136720 of 54,363 recalls

Medical DeviceApril 28, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Recalled by...

The Issue: Due to the buildup of grease within the hose and motor, the product may...

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

Class II — Potential Health HazardOngoing
DrugApril 27, 2016· Novo Nordisk Inc

Recalled Item: Norditropin FlexPro Somatropin (rDNA origin) injection Recalled by Novo...

The Issue: Defective Delivery System; may have a low frequency assembly fault which may...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 27, 2016· Teva North America

Recalled Item: Linezolid Injection Recalled by Teva North America Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Due to potential for leaking bags.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 27, 2016· Mighty Leaf Tea

Recalled Item: Mighty Leaf Tea Company Organic Ginger Peach Iced Tea Recalled by Mighty...

The Issue: Firm was notified by their supplier of Organic Ginger Peach tea that it has...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2016· Dessert Innovations II Candy Divison

Recalled Item: White Cupcakes with Yellow Icing Recalled by Dessert Innovations II Candy...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2016· Dessert Innovations II Candy Divison

Recalled Item: White Cupcakes with White Icing Recalled by Dessert Innovations II Candy...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2016· Dessert Innovations II Candy Divison

Recalled Item: White Cupcakes with Pink Icing Recalled by Dessert Innovations II Candy...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2016· Dessert Innovations II Candy Divison

Recalled Item: White Cupcakes with Blue Icing Recalled by Dessert Innovations II Candy...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 26, 2016· Greiner Bio-One North America, Inc.

Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...

The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· STERILMED, INC.

Recalled Item: Reprocessed Microline Scissor Tips intended to be used with a Recalled by...

The Issue: Sterlilmed is recalling all unexpired Scissor Tips because of a potential...

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2016· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine- MPF (Bupivacaine HCI Injection Recalled by Fresenius Kabi USA,...

The Issue: Presence of Particulate Matter: Glass particulate found in sterile...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· GSK Consumer Healthcare

Recalled Item: Breathe Right Clear Recalled by GSK Consumer Healthcare Due to Some cartons...

The Issue: Some cartons used in the secondary packaging of Breathe Right Clear, Large,...

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

Class III — Low RiskOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT-S(64) 4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing