Check a product

HeartSine distributed certain models of samaritan PAD defibrillators without a required Maintenance Supplement document. This document provides instructions for an additional quarterly (every 3 months) maintenance check beyond the standard monthly check. Without these instructions, facilities may not perform the full maintenance schedule needed to keep the devices in proper working order.

Moderate·FDA·Oct 7, 2026

The bolus tracking application on Philips Spectral CT 7500 scanners (Software V5.2.x) can malfunction and continue taking imaging shots even after reaching the contrast threshold. This can cause patients to receive unintended additional radiation during CT scans.

Moderate·FDA·Oct 7, 2026

Illumina has issued a retrospective correction for certain NovaSeq 6000Dx and DRAGEN Server instruments used in genetic testing. These devices contain a security vulnerability in the server component that could potentially allow unauthorized access. This affects 80 instruments distributed worldwide.

Moderate·FDA·Oct 7, 2026·Illumina

Mastisol Skin Adhesive, a sterile surgical glue used in regional anesthesia procedures, is being recalled due to manufacturing issues with the product contained in surgical convenience trays. The recall affects a specific lot used in continuous epidural trays distributed nationwide.

Moderate·FDA·Oct 7, 2026·Custom Interventional Pain Management

ASP Global is recalling 64 Expressaire disposable tourniquet cuffs made between September 2016 and March 2023. The labels list a 10-year shelf life, but the validated shelf life is 5 years, so the printed expiration dates are wrong. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·ASP Global64 products

Lior brand Cinnamon Ground Seasoning in 90g containers has been found to contain elevated levels of lead. The affected product has the code GAP11304 printed on the side of the container. About 162 cases were distributed across New York, New Jersey, Pennsylvania, Texas, Florida, and Illinois.

Moderate·FDA·Oct 7, 2026

Organiccs Absolutely Pure Type-1 Hydrolyzed Collagen Peptides contain undeclared shellfish (crab shell) from the glucosamine sulfate ingredient. People with shellfish allergies could have a serious allergic reaction if they use this product. The product was distributed primarily to medical offices in California, Oregon, Washington, Kentucky, Massachusetts, and Hawaii.

Moderate·FDA·Oct 7, 2026

Cloud Cafe branded Collagen Milk and Strawberry Milk Zero products contain fish that is not listed on the label. These products were distributed to a single Los Angeles distributor. The affected boxes have a Best By date of 5/13/2028.

Moderate·FDA·Oct 7, 2026·Cloud Cafe

Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil contains garlic essential oil that is not approved for use in food products. The affected oil was sold in 3.4 fl oz, 8.5 fl oz, and 17 fl oz bottles to consumers across multiple states. No illnesses have been reported.

Moderate·FDA·Oct 7, 2026·Kofinas

Some 12-ounce cans labeled as 7Up Tropical Zero Sugar actually contain full-sugar soda instead. This affects consumers who chose the zero-sugar version, particularly those managing sugar intake for health reasons like diabetes. The affected cans were distributed in Utah with a best-by date of March 17, 2027.

Moderate·FDA·Oct 7, 2026

Khazana Spice Magic Fennel Candy contains Yellow 5, Yellow 6, Red 3, and Blue 1 food dyes that were not declared on the label. These dyes can trigger allergic reactions or other health issues in people with sensitivities or those who avoid certain additives for medical or religious reasons.

Moderate·FDA·Oct 7, 2026

A batch of benzoyl peroxide wash distributed by Rugby Laboratories has been found to contain microbial contamination. The affected product is a 5% benzoyl peroxide topical wash in a 5 fl oz bottle, lot #0525-02-345, expiring 02/2027, distributed in Illinois only.

Moderate·FDA·Oct 7, 2026·SV Labs2 products

Apotex Corp. is recalling Paroxetine Extended-Release Tablets 37.5mg (Lot# TY9495, Exp Date 05/2027) because they failed to meet dissolution specifications. This means the tablets may not break down properly in the body, affecting how much medicine is absorbed.

Moderate·FDA·Oct 7, 2026

Par Health USA and Endo USA are recalling certain lots of Buprenorphine Hydrochloride 0.3 mg/mL injection due to crystallization in the vials. Crystallization can affect the drug's effectiveness and safety. The recall affects six specific lots distributed nationwide.

Moderate·FDA·Oct 7, 2026

A shipment of Zoladex (goserelin) 3.6 mg implants was left in an unheated FedEx trailer in outdoor conditions for approximately 25.5 hours. This temperature exposure may have affected the medication's stability and effectiveness. The recall affects 296 cartons with lot number YN0099 (expiration 01/31/2028).

Moderate·FDA·Oct 7, 2026·TerSera Therapeutics

Aurolab Trust FOCUS PI Hypromellose 0.7% eye drops (a sterile ophthalmic solution) failed to meet sterility standards during manufacturing. Two batches distributed in Virginia are affected. No injuries have been reported.

Moderate·FDA·Oct 7, 2026·Aurolab

Amneal Pharmaceuticals is recalling specific lots of Estradiol Gel 0.1% because some packets in affected cartons were found to be empty or only partially filled. This means patients may not receive the correct dose of medication. The recall affects 2,592 cartons distributed nationwide.

Moderate·FDA·Oct 7, 2026

Glenmark Pharmaceuticals received complaints that some cans of Clindamycin Phosphate Foam 1% arrived damaged and were leaking. The affected product was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 7, 2026

Ajanta Pharma USA Inc. is recalling one lot of Ranolazine Extended-Release Tablets, 1000 mg, because the tablets failed to meet dissolution specifications. This means the medication may not release properly in the body, potentially affecting its effectiveness. The recall affects lot DJ25134 with an expiration date of 11/30/2028, distributed nationwide.

Moderate·FDA·Oct 7, 2026

Canned chicken Vienna-style sausages branded Grace were illegally imported from Jamaica without U.S. food safety inspection. The products were distributed to stores in Alabama, Florida, Georgia, Maryland, and Texas. No illnesses have been reported.

Moderate·USDA·Oct 6, 2026·Grace

Certain 2024 Kovatch CV515 SFA 4x4 emergency vehicles have a component that may stop working, causing the exterior warning lights and emergency pump functions to fail. When these lights don't work, other drivers can't see the vehicle clearly, raising the risk of a crash. When the pump fails, emergency equipment may not operate properly.

Moderate·NHTSA·Oct 6, 2026·Kovatch Mobile Equipment Corp.

Certain 2025–2027 Ford F-150 vehicles have front seats that may not be properly bolted to the vehicle. If a seat is loose, it may not restrain occupants correctly during a crash, increasing injury risk.

Moderate·NHTSA·Oct 6, 2026

A component in the 2024 Metrostar emergency vehicle may fail, causing exterior lights and emergency pump functions to stop working. When exterior lights don't work, other drivers can't see the vehicle clearly, raising the risk of a crash. Loss of pump function could also delay use of emergency equipment.

Moderate·NHTSA·Oct 6, 2026·Spartan Fire, LLC

Certain 2026 Ram 2500 pickup trucks have a steering column control module that can fail, causing the electronic stability control system to stop working. This increases the risk of losing vehicle control and crashing.

Moderate·NHTSA·Oct 6, 2026

The rearview camera on certain 2015 Ford Transit Connect vehicles may display an inverted, distorted, intermittent, or blank image when in reverse. This reduced visibility behind the vehicle increases the risk of a crash.

Moderate·NHTSA·Oct 6, 2026

A software issue in the newest StatStrip Glucose Hospital Meter (Gen 2.0 model) can cause a glucose test result to be incorrectly linked to the wrong patient's medical record. When a patient ID barcode is scanned, previous patient information may stay on the meter screen; if a healthcare worker accidentally accepts it, the test result goes to the wrong patient, potentially leading to incorrect treatment decisions. One case of inappropriate insulin administration has been reported.

Moderate·FDA·Oct 5, 2026·StatStrip

Certain 2025–2027 Road Rescue and Wheeled Coach ambulances built by REV Ambulance Group Orlando may develop a faulty electronic node that disables warning lights. Without functioning warning lights, these ambulances are at increased risk of being involved in a crash.

Moderate·NHTSA·Oct 5, 2026·REV Ambulance Group Orlando, Inc.

Certain 2027 Forest River Surveyor recreational trailers have an exterior electrical outlet that is not wired to a GFCI (ground-fault circuit interrupter) circuit. Without GFCI protection, the outlet may fail to shut off power during an electrical ground fault, creating a shock hazard.

Moderate·NHTSA·Oct 5, 2026

Certain 2026–2027 Sunseeker, Solera, and Forester recreational vehicles have incorrect tire inflation information printed on the Federal Placard. Following this wrong information could lead to overinflated tires, which increases the risk of a crash.

Moderate·NHTSA·Oct 5, 2026

Certain 2018–2026 Motor Coach Industries buses have a dashboard indicator light that may not illuminate when hazard warning lights are on. This can cause drivers to forget to turn off exterior lights when they're no longer needed, which may confuse other drivers and increase crash risk.

Moderate·NHTSA·Oct 5, 2026·Motor Coach Industries, Inc