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Recall archive

95,413 stored notices, from Jun 20, 2012 to Nov 11, 2026.

32,363 recalls · page 23 of 1349

Medical devices

Reported Sep 16, 2026Updated Sep 22, 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 (openFDA device enforcement)

Food

Reported Sep 16, 2026Updated Sep 22, 2026

Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen

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

Euro Foods Group USA Nj Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 16, 2026Updated Sep 22, 2026

Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower, net wt. 3oz (85g). UPC 6 28634 44216 6. Ingredients:…

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

Exotique Foods Canada

FDA (openFDA food enforcement)

Food

Reported Sep 16, 2026Updated Sep 22, 2026

Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz

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

Ferrero USA

FDA (openFDA food enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

Bravo CF capsule delivery device, 5-pack, Product Number FGS-0635, Bravo CF capsule delivery device, 1-pack, Product…

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

Given Imaging Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Drugs

Reported Sep 16, 2026Updated Sep 22, 2026

Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only,…

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

ImprimisRx NJ LLC

FDA (openFDA drug enforcement)

Food

Reported Sep 16, 2026Updated Sep 22, 2026

Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506

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

International Sprout Holdings, Inc.

FDA (openFDA food enforcement)

Food

Reported Sep 16, 2026Updated Sep 22, 2026

Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold…

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

L-Nutra Inc.

FDA (openFDA food enforcement)

Drugs

Reported Sep 16, 2026

Apheresis Platelets, Leukocytes Reduced, Pathogen Reduced

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

Lifesouth Community Blood Centers - Montgomery Region

FDA (weekly enforcement report)

Drugs

Reported Sep 16, 2026

Apheresis Platelets, Leukocytes Reduced, Pathogen Reduced

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

LifeSouth Community Blood Centers, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy…

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

Lutronic Corporation

FDA (openFDA device enforcement)

Drugs

Reported Sep 16, 2026

Apheresis Platelets, Leukocytes Reduced, Irradiated

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

Medic Inc.

2 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 16, 2026Updated Sep 29, 2026

Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

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

Medical Action Industries, Inc. 306

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201

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

Nipro Renal Soultions USA, Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 16, 2026Updated Sep 29, 2026

fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City…

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

OurPharma LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

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

Stanford Blood Center LLC

1 more product in this recall

FDA (weekly enforcement report)

Drugs

Reported Sep 16, 2026

Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced

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

The American National Red Cross South Carolina Region

FDA (weekly enforcement report)

Drugs

Reported Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

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

The American National Red Cross

2 more products in this recall

FDA (weekly enforcement report)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B

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

Windstone Medical Packaging, Inc.

FDA (openFDA device enforcement)

Consumer products

Reported Sep 15, 2026Updated Oct 5, 2026

A&P Creations LLC recalls biQ-FEL biQ-FEL 500mL supplement bottle due to Product contains sildenafil and tadalafil

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

A&P Creations LLC

1 more product in this recall

FDA (recalls & safety alerts)

Food

Reported Sep 15, 2026Updated Oct 7, 2026

Danone USA recalls So Delicious Dairy Free Salted Caramel Cluster Non-Dairy Frozen Dessert pints due to Product may contain foreign objects such as small…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Danone USA

FDA (recalls & safety alerts)

Food

Reported Sep 15, 2026Updated Oct 7, 2026

Gias Foods, Inc. recalls Bettergoods Italian Lemon Alfredo Fettuccine due to Potential to be contaminated with Listeria monocytogenes

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Gias Foods, Inc.

FDA (recalls & safety alerts)

Drugs

Reported Sep 13, 2026Updated Oct 3, 2026

Centric Compounding LLC recalls Centric Compounding Compounded Glutathione 200 mg/mL 30 mL multidose vial; Myer’s Cocktail 30 mL multidose vial; Tri-Immune…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Centric Compounding LLC

FDA (recalls & safety alerts)

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