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 3066130680 of 49,744 recalls

FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Swirled Pretzels NET WT 5 OZ (141 g) packaged in foil bags...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 Recalled by Palmer and...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Creme De Menthe Bark Recalled by Palmer and Company, dba...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Christmas Tree Pretzel Recalled by Palmer and Company, dba...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Chocolate Pastel NP Pretzels NET WT 28 lbs (12.7 kg)...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: A) Peppermint Pretzels NET WT 5 OZ (141 g) Recalled by Palmer and Company,...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Cookies & Cream Bark Recalled by Palmer and Company, dba...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 9, 2017· Palmer and Company, dba Palmer Candy Co

Recalled Item: Palmer's Candies Bakery Delights Christmas Tree Pretzels NET WT 5 Recalled...

The Issue: Product contains an ingredient that was recalled by a supplier because it...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2017· Laerdal Medical Corporation

Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...

The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...

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

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2017· Hetero USA Inc

Recalled Item: Montelukast sodium tablets Recalled by Hetero USA Inc Due to Discoloration:...

The Issue: Discoloration: the firm received a complaint of a sealed bottle in which...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 6, 2017· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Oasis MRI System - C-Spine Coil Recalled by Hitachi Medical Systems...

The Issue: The customer indicated that the coil balun was hot to the touch when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2017· The See Clear Company

Recalled Item: Color contact lenses labeled under the following brands: Diamond Recalled by...

The Issue: Sterility and Misbranding: Lenses may not be sterile and may be labeled with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2017· C2 Therapeutics, Inc.

Recalled Item: C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller...

The Issue: The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2017· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...

The Issue: Products were made outside of Quality System Regulation, and potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2017· Haag-Streit USA Inc

Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...

The Issue: There is a possibility for data to be stored under the wrong patient on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...

The Issue: The company received a customer complaint for the inability to calibrate...

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

Class III — Low RiskOngoing
DrugJanuary 5, 2017· The Harvard Drug Group

Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2017· The Harvard Drug Group

Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Presence of Foreign Substance: consumer complaint for foreign matter...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2017· Endologix

Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...

The Issue: Endologix updated information on the rates of Type III endoleaks and...

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

Class II — Potential Health HazardOngoing