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 Sep 22, 2021

Configura Advance Chair, Model Number: CHAIR-0-SC1-030; Advance Chair, 100mm Castors, Std Backrest, Manual; Serial…

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

Accora Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

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

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

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

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Food

Reported Sep 22, 2021

Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.

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

Jimmy's Cookies, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

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

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 15, 2021

QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui…

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

Native Promotions, Inc.

FDA (openFDA drug enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

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

Hostess Brands, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 8, 2021

Cahill Cheddar with Porter PLU 93579 packaged in clear plastic

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

Whole Foods Market

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 1, 2021

Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…

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

Cardinal Health

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000,…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…

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

W. L. Gore & Associates Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700

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

Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

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

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;

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

Beckman Coulter Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License…

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"

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

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Aug 18, 2021

Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC,…

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

Eli Lilly & Company

FDA (openFDA drug enforcement)

Food

Reported Aug 18, 2021

Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested…

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

Iherb LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 18, 2021

Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Drugs

Reported Aug 18, 2021

C-PROGESTERONE OIL 100 MG/ML, 10 mL vials, Compound, People's Custom Rx, Compounded, Rx only, People's Custom Rx, 785 E…

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

People's Custom Rx and Clinical Care, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 11, 2021

GlideScope Go Monitors

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

Verathon, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 4, 2021

Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC …

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

Del Monte Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 4, 2021

OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic…

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

GE OEC Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery)…

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

Hill-Rom, 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.