All recall categories

Recalls distributed in Mississippi

These notices name Mississippi in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

2,477 stored notices name Mississippi, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Biomedical Division

FDA (openFDA device enforcement)

Food

Reported Nov 22, 2023

Guilt Free No Sugar Added Ice Cream Homemade Vanilla 1.5qts

High riskUsing this product could cause serious injury, illness or death — stop using it now.

TH Searcy LLC

FDA (openFDA food enforcement)

Food

Reported Nov 15, 2023

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

DJO EMPOWR Knee Punch Handle, REF: 801-05-040

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Family Dollar Stores, Llc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Gills Onions 3 lb. bags, diced yellow onions

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Gills Onions, LLC

72 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Percussionaire Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

Smiths Medical Portex Bivona Pediatric Tracheostomy Tube, Cuffless, Model 60P045, Sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

Astral 100 and Astral 150 ventilators

High riskUsing this product could cause serious injury, illness or death — stop using it now.

ResMed Ltd.

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Kroger Collard Greens packaged in plastic 16oz bag - 8 bags per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Kroger Co.

FDA (openFDA food enforcement)

Drugs

Reported Nov 1, 2023

Methotrexate Tablets, USP, 2.5 mg, 10x10 Unit-Dose Tablets per carton, Rx only, Distributed by: West-Ward…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

West-Ward Columbus Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 25, 2023

Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 18, 2023

CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RoyalVibe Health Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 11, 2023

REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson Infusion Therapy Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 11, 2023

Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Thoratec Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 4, 2023

Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 27, 2023

Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Sep 27, 2023

FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with SO SOFT* Lining, Orange, size small, Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

O&m Halyard, Inc.

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.