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 Apr 27, 2016
Acorn 180 Curved Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Apr 27, 2016
GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materne North America Corp.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
Extended Brilliance Workspace NM Nuclear medicine image display and processing application suite. AutoSPECT Pro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Bumble Bee Chunk Light Tuna in Water, 48cans/case, 5oz, UPC 8660000020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bumble Bee Foods LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 20, 2016
Diana Automated Compounding System, Diana Onco Plus, Item No. ASN220 The Diana is an automated compounding device for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Cittero Mortadella, packaged in deli bags. This is a deli service item.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bj Wholesale Club
70 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Scottcare Corporation
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2016
IMCO brand Conforming Stretch Gauze Bandages, 4 x 4.1 Yds/10 cm x 3,7 cm, Reorder No. 704-IMC, Bar code 6 86864 04351…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amd Ritmed
FDA (openFDA device enforcement)
Reported Apr 6, 2016
74" (188cm) approximately 9.0ml, 20 Drop Admin Set w/ Integrated ChemoLock Port sterile IV Administration sets are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
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)
Reported Apr 6, 2016
Cios Alpha, mobile X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
ShopRite Dry Roasted Unsalted Cashews 7 oz. (198 g) Distributed by Wakefern Food Corp., Elizabeth, NJ 07207 UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wakefern Foods Corp.
FDA (openFDA food enforcement)
Reported Mar 23, 2016
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Braga Organic Farms, Inc.
2 more products in this recall
FDA (openFDA food 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.