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.

2,512 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 Mar 26, 2014

Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a…

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

Philips Medical Systems North America Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated…

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2014

Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT

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

Zimmer, Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Navigator Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave…

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

Biomet 3i, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588.…

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

Clarity Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis IHC PR Breast Tissue Manual Read of Digital…

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

Leica Biosystems Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with…

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

Smith & Nephew Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2014

4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…

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

Smiths Medical ASD, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…

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

Elekta, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

BencoDental tartar & stain remover ultrasonic cleaning solution Product Usage: Formulated especially for removal of…

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

Heraeus Kulzer, LLC.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch…

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

Hospira Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes, 100 units/mL, 3 mL fill in a 12 mL…

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

Medefil Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

CSI, Diamondback 360 Coronary Orbital Atherectomy System, Part Number 70058-02, Model Number DBEC-125 Product Usage:…

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

Cardiovascular Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…

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

Ortho-Clinical Diagnostics

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Single and Dual use Emission Computer Tomography gamma cameras (BrightView XCT, BrightView X & BrightView SPECT)…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The…

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

Philips Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System

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

Smith & Nephew Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered,…

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

Winco Mfg., LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2014

Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK.…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2014

Dried Tapioca Pearl, Net Wt. 7oz, 50 bags/carton, UPC Code 0893467803068

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

New Japan International, Inc.

FDA (openFDA food 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.