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. 2,489 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,489 in last 12 months

Showing 2256122580 of 49,744 recalls

Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Dornier Medtech America, Inc.

Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...

The Issue: Pin hole package failures compromising sterility of product

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

Class II — Potential Health HazardOngoing
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Banana Bread Mix 14oz Recalled by Wholesome Treats, Inc....

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Classic Herb Bread Mix 19oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Yeast Free Bread Mix 18.1oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Black Bean Brownie Mix 14oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 31, 2019· Integra Limited

Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...

The Issue: Stability did not meet acceptance criteria for visual appearance during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief Recalled by...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
DrugMarch 29, 2019· X-Gen Pharmaceuticals Inc.

Recalled Item: Clonidine HCL Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Label Error on Declared Strength: Side carton panel incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: Discoloration: Expansion of an earlier recall due to the presence of dark...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 29, 2019· PROVIDENCE MEDICAL TECHNOLOGIES

Recalled Item: Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by...

The Issue: There may be dimensional manufacturing error that represents a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Prestilix 1600X Prestilix system is a fully integrated remote controlled...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Silhouette VR This fully integrated system offers intuitive controls with...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Proteus XR/a The Proteus XR/a radiographic system offers the flexibility...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Conformis, Inc.

Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-010101 Recalled by...

The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...

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

Class II — Potential Health HazardOngoing