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. 1,862 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,862 in last 12 months

Showing 3218132200 of 54,363 recalls

Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Best Practice Kit Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: USPACK-SUTURE KIT Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH Recalled by Medtronic Due...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R Recalled by Medtronic Due to...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Cook Inc.

Recalled Item: Vue Optic Visualization Source Recalled by Cook Inc. Due to Cook Inc. is...

The Issue: Cook Inc. is initiating a voluntary recall of the Vue Optic Visualization...

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

Class II — Potential Health HazardOngoing
DrugMay 2, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Famotidine for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc....

The Issue: CGMP Deviations

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

Class III — Low RiskOngoing
Refund
FoodMay 2, 2017· HVF Inc. d.b.a Huson Valley Farms

Recalled Item: Nutty INFUSIONS Roasted Cashew Butter Recalled by HVF Inc. d.b.a Huson...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2017· HVF Inc. d.b.a Huson Valley Farms

Recalled Item: Nutty INFUSIONS Ginger Wasabi Cashew Butter Recalled by HVF Inc. d.b.a Huson...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2017· U S Deer Antlers Export & Import

Recalled Item: Herbal Tea Variety 120 ml/pouch Recalled by U S Deer Antlers Export & Import...

The Issue: US Deer Antler Export and Import is recalling a variety of Herbal Teas...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 2, 2017· GE Healthcare, LLC

Recalled Item: Carestation 620 A1 Recalled by GE Healthcare, LLC Due to Carestation 620,...

The Issue: Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD Recalled by...

The Issue: Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· Hitachi Medical Systems America Inc

Recalled Item: Arietta 70 Ultrasound System Intended for use by trained personnel (doctor...

The Issue: The strength of the arm mounting mechanism was insufficient and had to be...

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

Class II — Potential Health HazardOngoing
DrugMay 1, 2017· Allergan Sales, LLC

Recalled Item: Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic...

The Issue: Failed Impurities/Degradation Specifications: stability testing results did...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2017· Herbalife International Of America Inc

Recalled Item: Protein Bar 14 bars/box Recalled by Herbalife International Of America Inc...

The Issue: Herbalife is recalling Protein Bar-Peanut Butter because it may contain a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 1, 2017· Zimmer Biomet, Inc.

Recalled Item: ROSA Brain 3.0 Stereotaxic instrument Computer-assisted surgical device....

The Issue: Robot arm being sent to the wrong position

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Zimmer Biomet, Inc.

Recalled Item: ROSA Spine 1.0.2 Stereotaxic instrument Computer-assisted surgical device....

The Issue: Robot arm being sent to the wrong position

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO 500 TUS-A500 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: XARIO 200 TUS-X200 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: XARIO 100 TUS-X100 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing