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 Feb 1, 2023
Wegmans Organic Farm & Orchard Micro Greens; 1.75 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2023
ACME Smoked Nova Salmon Net Wt. 4 OZ (113G) UPC: 23384104065
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lidl US TRADING
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2023
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
Centricity PACS-IW with Universal Viewer version 5.0. Used to display medical images (Including mammograms) and data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
14 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Weis Markets, Inc., Ice Cream Division
FDA (openFDA food enforcement)
Reported Dec 7, 2022
Alcon Custom Pak Surgical Procedure Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Dec 7, 2022
Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. individually wrapped plastic packages - 12 units per case UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amys Kitchen Inc.
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iRhythm Technologies, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Sedecal Soltus Battery Mobile X-Ray System REF Soltus 450 Battery Mobile X-Ray System REF Soltus 500
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal Sa
FDA (openFDA device enforcement)
Reported Nov 9, 2022
BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2022
Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bella Brands, LLC dba Bella Cucina Artful Food
13 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 9, 2022
Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 2, 2022
CorVocet Biopsy System/Catalog Code: CORA1610/B, CORA1610S/B, CORA1615/B, CORA1810/A, CORA1810/B, CORA1810S/B,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 2, 2022
THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Chai Box
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 2, 2022
AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Circulation, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2022
Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2022
Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods (Corporate Offices)
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2022
Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lyons Magnus LLC
11 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.