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 3676136780 of 54,363 recalls

Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

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

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

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

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow Edge-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TV Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Arthrex, Inc.

Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...

The Issue: Potential for polystyrene particulate presence.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 40 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 40 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Arthrex, Inc.

Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...

The Issue: Potential for polystyrene particulate presence.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Arthrex, Inc.

Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...

The Issue: Potential for polystyrene particulate presence.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Arthrex, Inc.

Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...

The Issue: Potential for polystyrene particulate presence.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Arthrex, Inc.

Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...

The Issue: Potential for polystyrene particulate presence.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Arthrex, Inc.

Recalled Item: BioSync Anatomic Cotton Wedge Recalled by Arthrex, Inc. Due to Potential for...

The Issue: Potential for polystyrene particulate presence.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Natus Medical Incorporated

Recalled Item: Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model Recalled...

The Issue: The replacement HEPA Filters have been manufactured with sealant that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: Streamline OCT Occipito-Cervico-Thoracic System Recalled by RTI Surgical,...

The Issue: Potential for a product defect where the cannula may be obstructed. This...

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

Class II — Potential Health HazardOngoing
FoodApril 21, 2016· CSM Bakery Products NA

Recalled Item: Yeast Roll Mix Recalled by CSM Bakery Products NA Due to Undeclared Allergen

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 21, 2016· CSM Bakery Products NA

Recalled Item: BM Westco Sup-R-Roll Donut Mix Recalled by CSM Bakery Products NA Due to...

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 21, 2016· CSM Bakery Products NA

Recalled Item: Buffets Corn Muffin Mix Recalled by CSM Bakery Products NA Due to Undeclared...

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