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 Oct 31, 2018

Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the…

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

Ecolab Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…

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

Medtronic Navigation, Inc.-Littleton

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

APTIO INPUT/OUTPUT MODULE

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

Siemens Healthcare Diagnostics, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…

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

GE Medical Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 24, 2018

Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - 888849000494 12 ct. Box UPC # - 888849000500

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

Quest Nutrition, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2018

Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

Colpo-Pneumo Occluder, Part CPO-6

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Hodgson Mill Cookie Mix Gluten Free 12oz. cardboard carton retail unit; 6 retail units per case. UPC Code 0 71518 02125…

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

Hodgson Mill Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 17, 2018

NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…

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

Neomed Inc.

FDA (openFDA device enforcement)

Drugs

Reported Oct 17, 2018

Actoplus met XR (pioglitazone and metformin HCl, extended-release) tablets, 15 mg/1000 mg, Rx Only, 30 tablet bottle,…

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

Takeda Development Center Americas, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 10, 2018

ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…

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

Endologix

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 10, 2018

ICU Medical 14" (36 cm) Appx 3.6 ml, Bifuse Transfer Set w/Rotating Luer, REF: 14237-28 The Intravascular…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 10, 2018

EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…

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

Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

ESSENTIO Pacemaker

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

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 3, 2018

FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483…

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

Confidence Inc./Confidence U.S.A. Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 3, 2018

Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…

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

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Medical devices

Reported Oct 3, 2018

INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…

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

Philips Electronics North America Corporation

26 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

Endoscopic Cleaning Brush, single use, sold in kits and labeled as the following: a. Item Number DYK1002DCB, BRUSH,…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 26, 2018

DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries

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

Pro-Med Instruments GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 19, 2018

Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. 6 OZ paper bag Dewey's BAKERY WINSTON-SALEM, NC…

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

Dewey's Bakery, Inc. dba Salem Baking Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 19, 2018

da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 19, 2018

Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280

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

Zimmer Biomet, Inc.

128 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 12, 2018

Foundation Modular Femoral Stem, Part Number, 220-10-110. Knee prosthesis component. The Foundation Revision Knee is a…

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

Encore Medical, LP

FDA (openFDA device 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.