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.
1,727 stored notices name Delaware, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Delaware too — those are in the archive.
Reported Jul 3, 2013
MAQUET GETINGE GROUP Arterial Cannula OD Used to introduce blood and sterile solutions into the systemic circulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Jul 3, 2013
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrad Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Wawa Black Forest Ham and Cheese on a Pretzel Roll with swiss cheese and country dijon honey mustard. Net Wt. 8.7 oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms New Jersey, NJ
FDA (openFDA food enforcement)
Reported Jun 26, 2013
Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Jun 26, 2013
Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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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.