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 48,100 notices were distributed nationwide, so they reach Delaware too — those are in the archive.
Reported Nov 11, 2020
Rice Pudding 5lb plastic containers. UPC: 4428421260. Refrigerated 34¿F-38¿F
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spring Glen Fresh Foods
FDA (openFDA food enforcement)
Reported Nov 4, 2020
Gracie's Pointe frozen raw shrimp. 1. 8/12 Count Per Pound Tail On, UPC: 849558095034 2. 21/25 Count Per Pound Tail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capital Seaboard
FDA (openFDA food enforcement)
Reported Nov 4, 2020
Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nurture Inc. dba Happy Family
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 4, 2020
5.5MM Arthrogarde Hip Access Cannula
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2020
NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
98 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
40 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Langston Dual Lumen Catheter
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Shirakiku brand Black Fungus (Kikurage); 5 lb. bag, 6 x 5 lb. bags per case Item # 60403; UPC 0 74410 60403 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2020
AquaBplus and AquaBplus B2 Water Purification System. For use with a hemodialysis system to remove organic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2020
ADVIA Chemistry Systems-Fructosamine (FRUC)-For in vitro diagnostic use in the quantitative measurement of glycated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2020
SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
FDA (openFDA food enforcement)
Reported Oct 7, 2020
Pacific Xtreme (PTCA Balloon Dilation Catheter)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ev3 Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Speed Stitch Needle Cassette
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Panther Fusion Tube Tray, Part: FAB-15004, REF: PRD-04000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Red Onions, Bulk
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lancaster Foods LLC
FDA (openFDA food enforcement)
Reported Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Merge PACS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 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.