All recall categories

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.

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 8, 2023

Wegman's Organics Sweet Kale Chopped Salad Kit, 8oz.

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

Braga Fresh Foods

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a…

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

Maquet Cardiovascular, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor

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

Orgain

FDA (openFDA food enforcement)

Medical devices

Reported Oct 11, 2023

Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic Navigation System - 230V 50Hz SYS-4000 SPiN…

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

Olympus Corporation of the Americas

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 11, 2023

Heartmate 3 LVAS Implant Kit, REF: 106524US, 106524INT; Heartmate XVE & HeartMate II Apical Coring Knife, REF: 1050

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

Thoratec Corp.

FDA (openFDA device enforcement)

Food

Reported Oct 4, 2023

Weis Quality Brownie Moose Tracks Ice Cream (48oz)UPC of 041497-01194 Packaged in a scround container. 6 units per case.

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

Weis Markets, Inc., Ice Cream Division

FDA (openFDA food enforcement)

Medical devices

Reported Sep 27, 2023

Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Sep 27, 2023

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…

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

Abbott Medical

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

ACUSON Redwood 2.0 ultrasound systems, REF: 11503314

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 Sep 13, 2023

Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous retrieval of cardiac leads.…

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

Cook Vandergrift, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 13, 2023

ISee Ortho-K Lens

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

PARAGON VISION SCIENCES, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 13, 2023

Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plastic tubs; and Tippy Toes brand…

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

PBM Nutritionals, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2023

Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 6, 2023

epoc BGEM BUN Test Card with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor Configuration 41.1

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

Siemens Healthcare Diagnostics Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2023

Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15129-0 Soft Serve on the Go brand Parve…

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

Real Kosher Ice Cream, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2023

TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT, REF 71647336, Femur nail

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

Smith & Nephew, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 23, 2023

Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.

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

Lidl US TRADING

FDA (openFDA food enforcement)

Food

Reported Aug 16, 2023

Caramel Butter Pecan Cup 14 fl oz. cup (8 per case) Paper cup with paper lid Brand: Eclipse Foods UPC: 810049270490…

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

Eclipse Foods Co.

FDA (openFDA food enforcement)

Free recall alerts

Get alerted about new Delaware recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Other states

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.