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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.

2,512 stored notices name Mississippi, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Medical devices

Reported Feb 21, 2018

EMS products from Graham Medical, SnugFit(R) Expandable Mattress Cover, Code 72930, UPC 1 07 47036 72930 3

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

Little Rapids Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…

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

Zimmer Surgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2018

ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Food

Reported Feb 14, 2018

Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz…

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

Chobani

FDA (openFDA food enforcement)

Medical devices

Reported Feb 14, 2018

SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 14, 2018

SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Drugs

Reported Feb 7, 2018

Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064,…

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

AbbVie Inc.

FDA (openFDA drug enforcement)

Food

Reported Feb 7, 2018

Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100…

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

Dollar General Corporation, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2018

Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…

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

Ormco/Sybronendo

FDA (openFDA device enforcement)

Medical devices

Reported Feb 7, 2018

Syngo.plaza Picture Archiving and Communication System (PACS) with software version VB20A; Model numbers: 10863171,…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2018

Syngo Imaging version V31 (model # 10014063) is a Picture Archiving and Communication System (PACS) intended to…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 24, 2018

ACCOLADE SR Pacemaker

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

Boston Scientific Corporation

23 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jan 24, 2018

Rich Products Corporation Retira Productos De Carne De Res Debido A Una Posible Contaminacin Con Listeria

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

Recalling firm not stated

USDA FSIS

Medical devices

Reported Jan 24, 2018

Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic,…

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

Owen Mumford USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2018

Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant…

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

Cordis Corporation

FDA (openFDA device enforcement)

Food

Reported Jan 17, 2018

365 brand Egg Nog, Grade A; 1 qt. and 1/2 GAL; and Harrisburg Dairies brand Egg Nog, Grade A; 1/2 GAL, 1 Quart, 16 FL.…

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

Harrisburg Dairies, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2018

UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z,…

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

King Systems Corp. dba Ambu, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2018

Sundream 12 V tanning bed

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

ProSun International, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2017

Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 20, 2017

Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments.

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

Elekta Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 20, 2017

ABL800 analyzer with FLEXQ module. Device intended for in vitro testing of samples of whole blood for the parameters…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2017

TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep…

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

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 13, 2017

Comforts FOR BABY Purified Water with Flouride Added. 1 GAL (3.78 L) DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO…

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

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Dec 6, 2017

Dark Chocolate Almond, Net 11 oz., Contains Almond and Soy, Distributed By: Dutch Valley Food Distributors, Inc.,…

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

Dutch Valley Food Distributors Inc.

1 more product in this recall

FDA (openFDA food enforcement)

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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.