Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,448 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,448 in last 12 months

Showing 2940129420 of 49,744 recalls

Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT 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· 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
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
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· 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
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 Recalled by Toshiba...

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: APLIO 300 TUS-A300 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· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Set Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing