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. 1,755 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,755 in last 12 months

Showing 4526145280 of 54,363 recalls

Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Innovasis, Inc

Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling

The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...

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

Class II — Potential Health HazardOngoing
DrugJuly 3, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Metoprolol Succinate Extended-release Tablets Recalled by Mylan...

The Issue: Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Failed PH Specifications: It has been determined that the pH of the lots...

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

Class III — Low RiskOngoing
Refund
DrugJuly 3, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJuly 3, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Failed PH Specifications: It has been determined that the pH of the lots...

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

Class III — Low RiskOngoing
Refund
FoodJuly 3, 2014· Metagenics, Inc.

Recalled Item: UltraBalance Protein Powder Recalled by Metagenics, Inc. Due to Undeclared Soy

The Issue: Metagenics is recalling UltraBalance Protein powder because it may contain...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2014· CooperSurgical, Inc.

Recalled Item: CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/...

The Issue: Unsealed pouches.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Intelerad Medical Systems

Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...

The Issue: In specific situation a partially truncated file may be written to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve only with SIPHONGUARD¿ Device Recalled by...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with Catheter and Accessories Recalled by...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing