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 Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2019

Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…

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

ICU Medical Inc.

21 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2019

AIR Technology Anterior Array, Catalogue Numbers: (a) 5746694, (b) 5746695, (c) 5746696, a receive-only RF coil…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2019

Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502

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

Roche Diagnostics Operations, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2019

L5C4531 X1 Integrated APD Set with Cassette 3-Prong Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal…

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

Howmedica Osteonics Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 2, 2019

Udi's Classic Hamburger Buns, packaged in a 10.4 oz. plastic bag, with eight bags per wholesale case. UPC…

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

ConAgra Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 2, 2019

Gold Cup Leadwire and Snap Leadwire with the following component descriptions: 1. 24" Snap Leadwire, Blue; 2. 40" Snap…

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator

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)

Meat & poultry

Reported Sep 20, 2019

Astrochef LLC. Retira Platos Preparados De Pollo Estilo Pub Debido A Un Error De Rotulación Y Alérgenos No Declarados

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

Pegasus Foods Inc.

USDA FSIS

Medical devices

Reported Sep 18, 2019

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…

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

Allergan PLC

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can

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

Natures One Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 11, 2019

Norm-O-Temp model 111Z

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

Cincinnati Sub-Zero Products LLC, a Gentherm Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

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

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

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)

Food

Reported Aug 21, 2019

Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…

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

BIMBO Bakeries USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2019

SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System

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

Pega Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2019

Great Value Mild Taco Seasoning, Net Wt. 1 OZ, Distributed by Wal-Mart Stores, Inc. Bentonville, AR. UPC 0 78742 24572v0

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

CH Guenther & Sons, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 14, 2019

The Visibly Online Refractive Vision Test which is part of the Visibly Vision Test Solution, This is a software…

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

Opternative Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

ELLIPSE VR, REF: CD1377-36C Implantable cardioverter defibrillators (ICDs)

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

St Jude Medical Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 7, 2019

Maximum Pelvic Trainer (MPT)

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

Ralston Group

FDA (openFDA device enforcement)

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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.