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TradepilotUSA Recalls

TradePilot Recalls

Official product recall notices and clearly labeled enforcement reference records.

Reference notice · drug

Sterling Pharmaceutical Services LLC — Walgreens Lubricant Eye Drops, 0.5 FL OZ (15 mL) 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by Walgreens Co., 200 Wilmot Road, Deerfield, IL 60015, NDC 0363-8833-15.

Lack of Assurance of Sterility

Dupo, IL, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · drug

Macleods Pharmaceuticals Limited — Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ, 08540; Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Him

Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification.

Tehsil Baddi, District Solan, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · drug

Sterling Pharmaceutical Services LLC — TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company

Lack of Assurance of Sterility

Dupo, IL, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · drug

Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company — Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist

Lack of Assurance of Sterility

Tarrytown, NY, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · food

WWF Operating Company — So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. 16 oz paper tub with an attached paper lid. Sold as a single unit multi serving tub. UPC 744473

Product may contain foreign material: small stones and other hard objects.

Louisville, CO, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — food enforcement reference

Reference notice · drug

Sterling Pharmaceutical Services LLC — AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops, Sterile, 0.5 FL OZ (15 mL) EACH, 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by: AVK

Lack of Assurance of Sterility

Dupo, IL, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · food

United Sugar Producers and Refiners — Powdered Sugar, Packaged in the following configurations: 1. United 6X, Net Wt. 50 lbs. (22.68kg), Item Number 810087. UPC 7 85921-07090 4. Distributed by: United Sugar Producers &

Potential Wheat Kernel contamination.

Minneapolis, MN, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — food enforcement reference

Reference notice · food

GIAS FOOD INC. — Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22

Contamination with Listeria monocytogenes

New York, NY, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — food enforcement reference

Reference notice · food

United Sugar Producers and Refiners — Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051. Distributed By: United Sugar Producers & Refiners, Minneapolis,

Potential Wheat Kernel contamination.

Minneapolis, MN, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — food enforcement reference

Reference notice · drug

Amneal Pharmaceuticals of New York, LLC — Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahme

Defective Delivery System: Possibility of no medication in the prefilled pen.

Brookhaven, NY, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · drug

Sterling Pharmaceutical Services LLC — Reliable -1 Laboratories, Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY,

Lack of Assurance of Sterility

Dupo, IL, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — drug enforcement reference

Reference notice · food

Kwok Shing, Inc. — American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET WT. 8 oz.

Potential contamination with pesticides.

San Francisco, CA, US · Updated 9/30/2026, 12:00:00 AM UTC

Source: FDA — food enforcement reference

Reference notice · device

Olympus Corporation of the Americas — Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih OLYSENSE Hub System

While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.

Center Valley, PA, US · Updated 9/29/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Philips North America Llc — Philips Medical Systems Technologies Ltd. Spectral CT 7500, Software V5.2.x, Product Code 728333

The Bolus tracking scan application may crash with a system error message. Bolus Tracker shots may continue to occur even if the contrast threshold is reached. This may result in the patient receiving additional radiation.

Cambridge, MA, US · Updated 9/29/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — Intrapulmonary Percussive Ventilation, IPV-2C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used with Instruction Manual

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — In-Line Valve, Product Number: P5-TEE

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with Instruction Manual

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number: P5-UC, used with In-Line Valve Instructi

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Percussionaire Corporation — Intrapulmonary Percussive Ventilation, IPV-1C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used with Instruction Manual

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycard…

Sandpoint, ID, US · Updated 9/28/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

American Nitrile Operations Llc — Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number: 72-50900, 72-50901, 72-50902, 72-50903, 72-50904 Product Description: Blue Nitrile Patient examina

Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.

Grove City, OH, US · Updated 9/25/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Cardinal Health 200, LLC — Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT,GU DAVINCI , Catalog Number: PGVMDVBWU; 2) KIT,GU DAVINCI , Catalog Number: PGVMDVBWV; 3) KIT,GU DAVINCI

The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.

Waukegan, IL, US · Updated 9/25/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Shanghai United Imaging Healthcare Co., Ltd. — Computed Tomography X-ray System, Model: uCT 550 with software

Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.

Shanghai, US · Updated 9/25/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

Reference notice · device

Alere San Diego, Inc. — Fisher Scientific Sure-Vue Urine hCG, Model/ Part: FHC-102/23900526; Henry Schein, Inc. One Step + Urine Cassette Test, Model/ Part: FHC-102/9004074, FHC-102/9004073; Alere hCG Cas

hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.

San Diego, CA, US · Updated 9/25/2026, 12:00:00 AM UTC

Source: FDA — device enforcement reference

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