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Recalls distributed in Delaware

These notices name Delaware 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.

1,697 stored notices name Delaware, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Delaware too — those are in the archive.

Medical devices

Reported Jun 26, 2013

GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2013

TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1 Tissue Removal System is indicated for use in…

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

American Optisurgical Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2013

XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…

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

Atlantic Pro Nutrients, Inc. dba XYMOGEN

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2013

embla Embletta Gold (It functions as a Polysomnography Recorder and Ventilator Effort Recorder). The Embletta Gold is a…

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

Embla System LLC

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2013

Chicken Noodle Soup Mix, "9 oz cello bag, Contents: All natural enriched semolina flour***PURELY AMERICAN 5991…

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

Purely American, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2013

BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…

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 Jun 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…

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

Orthovita, Inc., dba Stryker Orthobiologics.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…

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

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…

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 May 22, 2013

AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control System is used to treat urinary incontinence due to…

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

American Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

Fluoroscan Mini C-arm InSight, software versions 1.x, 2.x, 3.x The device is a Mini C-arm Fluroscopic Imaging System…

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

Hologic, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…

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

Olympus America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters (with ultrasound) Product Code: PE623 Sure-Pro¿ Embryo…

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

Smiths Medical ASD, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…

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

Advanced Sterilization Products

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis…

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries Model number: HT70 and HT70 Plus. The…

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

Newport Medical Instruments Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2013

Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Term Monitoring system (Models HSYS-REC-WD, HSYS-REC-WT;…

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

Stellate Systems

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2013

EVOTECH Endoscope Cleaner & Reprocessor System, P/N 50004 Designed to automatically clean and high-level disinfect…

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

Advanced Sterilization Products

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2013

Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 24, 2013

Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R)…

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 Apr 17, 2013

LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit…

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

Lighthouse For The Blind

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2013

Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715,…

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

Medtronic MiniMed

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2013

Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the determination of the activated partial thromboplastin time…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 17, 2013

CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542,…

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

Thermo Fisher Scientific (Asheville) LLC

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.