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. 2,502 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,502 in last 12 months

Showing 2034120360 of 49,744 recalls

DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2019· Images Unlimited Products, dba Cellect Products

Recalled Item: CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered...

The Issue: Product contains unsafe levels of Arsenic and Lead

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Epic Pharma, LLC

Recalled Item: Estradiol tablets Recalled by Epic Pharma, LLC Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: Estradiol 1 mg was found in a 100...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Alkermes, Inc.

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...

The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...

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

Class III — Low RiskOngoing
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 24, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to SOMATOM...

The Issue: SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT...

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

Class II — Potential Health HazardOngoing
DrugSeptember 23, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Tablets USP Recalled by AuroMedics Pharma LLC Due to CGMP...

The Issue: CGMP DEVIATIONS: One lot of Ranitidine Tablets USP, 150 mg is being recalled...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2019· Unipharma, Llc.

Recalled Item: DrKids Himasal Natural Nasal Saline Solution Recalled by Unipharma, Llc. Due...

The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 150mg 500 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Morton Grove...

The Issue: Failed Impurities/Degradation Specifications - failed specs for Prednisolone...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only...

The Issue: CGMP Deviations: Detection of a trace amount of an unexpected impurity,...

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

Class II — Potential Health HazardOngoing
Refund