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. 1,085 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,085 in last 12 months

Showing 14921–14940 of 54,363 recalls

Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...

The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2021· ev3 Inc.

Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...

The Issue: Reports have been received of tip damage during use of the devices which...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 6, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...

The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2021· ev3 Inc.

Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...

The Issue: Reports have been received of tip damage during use of the devices which...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 6, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...

The Issue: There is a software issue associated with the ability to properly complete a...

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

Class II — Potential Health HazardOngoing
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Mitomycin-C Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen Recalled by...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Extra Strength Headache (acetaminophen 250 mg Recalled by Medique Products...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Valisa MFG LLC

Recalled Item: kleantouch HAND SANITIZER (ethyl alcohol 70%) Recalled by Valisa MFG LLC Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Medique Pain-Off (Acetaminophen 250 mg Recalled by Medique Products Due to...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl/Tropicamide Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Dibutyl Squaric Acid Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl/Tropicamide/Cyclopentolate HCl/Ketorolac Sterile...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl 0.5 mg/5mL Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Cantharidin Gel-Forming Suspension Recalled by Edge Pharma, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Methacholine Challenge 5-Syringe Test Kit Recalled by Edge Pharma, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund