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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.

Medical devices

Reported Sep 23, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

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

Bard Access Systems, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

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

Bd Switzerland Sarl

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

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

Happiest Baby, Inc.

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Plum administration sets

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

ICU Medical, Inc.

7 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software…

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

Nuclein LLC

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026

Philips Patient Information Center iX REF:866389

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

Philips North America

1 more product in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 16, 2026

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…

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

C.R. Bard Inc.

5 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:…

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

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 9, 2026Updated Sep 16, 2026

Food to Live brand Organic Supergreens mix (kale, moringa leaf, wheat grass, & spirulina), 8 oz, 1 lb, 1.5 lb, 3 lb, 6…

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

Lexunder Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Velys Enabling Tech Robotic-Assist Station REF: 451611001

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

Medos International Sarl

FDA (openFDA device enforcement)

Food

Reported Sep 2, 2026Updated Sep 13, 2026

Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…

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

Byron White Formulas, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 2, 2026Updated Sep 7, 2026

ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with coconut sprinkles. Product is…

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)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710,…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTRIBUTED BY LIDL US, LLC ARLINGTON, VA…

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

Lidl US TRADING

FDA (openFDA food enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

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

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

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

SDI Limited

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Sep 7, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

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

Erbe USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product…

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: -…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…

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

Contego Medical, Inc.

FDA (openFDA device enforcement)

Consumer products

Reported Aug 12, 2026Updated Sep 16, 2026

Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…

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

KAO USA Inc.

FDA (weekly enforcement report)

Medical devices

Reported Aug 12, 2026

Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530…

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

Maquet Critical Care AB

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…

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

Pride Mobility Products Corp.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 5, 2026

DQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L). Keep refrigerated.

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

Galliker Dairy Co., Inc.

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.