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. 2,465 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,465 in last 12 months

Showing 2404124060 of 49,744 recalls

DrugAugust 23, 2018· Hellolife

Recalled Item: Compulsin Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· Hellolife

Recalled Item: Neuroveen Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· Hellolife

Recalled Item: Thyroveev Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· Pfizer Global Supply

Recalled Item: Children s Advil Suspension Ibuprofen Oral Suspension Recalled by Pfizer...

The Issue: Labeling Error: Not elsewhere classified. product has a dosage cup marked in...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 23, 2018· Dewey's Bakery, Inc dba Salem Baking Company

Recalled Item: Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. Recalled...

The Issue: The firm was notified by a customer that mold was in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...

The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2018· Becton Dickinson & Company

Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...

The Issue: One lot of the specified needles is not performing as intended due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...

The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Recalled...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp :...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
DrugAugust 21, 2018· Sichuan Friendly Pharmaceutical Co.,Ltd.

Recalled Item: Thyroid Powder 25kg/drum Recalled by Sichuan Friendly Pharmaceutical...

The Issue: CGMP Deviations: Thyroid Powder has inconsistent levels of the active...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Accord Healthcare, Inc.

Recalled Item: Hydrochlorothiazide Tablets USP Recalled by Accord Healthcare, Inc. Due to...

The Issue: Product Mix-Up: customer complaint that a sealed bottle labeled as...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Methyl-Cobalamin injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Mayne Pharma Inc

Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Mayne Pharma Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is...

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

Class III — Low RiskOngoing
Refund
DrugAugust 21, 2018· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP 100 mL bags Recalled by Baxter Healthcare...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Methyl-Cobalamin injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund