All recall categories

Recalls distributed in Louisiana

These notices name Louisiana 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.

3,284 stored notices name Louisiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Louisiana too — those are in the archive.

Medical devices

Reported Oct 8, 2014

Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…

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

Instrumed International, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical…

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2014

Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is designed for use on patients who require…

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

CareFusion 203, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a…

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

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 1, 2014

Oriya organics Superfood Protein Medley Sprouted Chia Seeds Spirulina Sprouted Brown Rice Protein Hemp Protein…

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

Oriya Organics

FDA (openFDA food enforcement)

Medical devices

Reported Oct 1, 2014

The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)]…

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

Peters Surgical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

No packaging. The device is a computed tomography scanner. Intended to provide corss sectional images of the human body…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level /…

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

Synthes, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455

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

Vidacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Ultraslim. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed,…

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

Advanced Photonic Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.

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

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below JResultNet is a stand-alone software package…

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

Data Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

BD Vacutainer Serum Tubes (RED TOP PLAIN TUBE 6.0 ML)Part Number: BD 367815 FMC Part Number: 87-7815-4 Single use tube…

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

Fresenius Medical Care Holdings, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…

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

GF Health Products, Inc./d.b.a.Basic American Metal Products

FDA (openFDA device enforcement)

Food

Reported Sep 24, 2014

Lean Cuisine Culinary Collection Chicken with Peanut Sauce. Packaged in 9 oz (255g) Plastic Tray in Fiberboard Carton…

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

Nestle USA, Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 24, 2014

Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…

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

Swanson Health Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2014

PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE; the Airway Gas Option N-CAiO and…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2014

Roche cobas IT 1000 Product Usage: Intended Use: An electronic device intended to store, retrieve, and process…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2014

PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…

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

Zimmer, Inc.

9 more products in this recall

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.