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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

31,892 recalls · page 59 of 1329

Drugs

Reported Apr 8, 2026

Prazosin Hydrochloride Capsules, USP, 1mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ,…

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

Appco Pharma LLC

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 8, 2026

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

BD Kiestra" ReadA; Catalog No.: 446948.

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

Bd Kiestra Lab Automation

FDA (openFDA device enforcement)

Drugs

Reported Apr 8, 2026Updated Sep 18, 2026

Blaine Labs, Inc. recalls Revitaderm, Tridergel Antiseptic wound care gel bottles and tubes due to Products were found to contain Lysinibacillus fusiformis, an…

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

Blaine Labs, Inc.

FDA (recalls & safety alerts)

Medical devices

Reported Apr 8, 2026

Burlington Medical, Thyroid Shield.

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

Burlington Medical, LLC

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777

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

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149

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

Civco Medical Instruments Co. Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

SIGNA Premier systems

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

GE Healthcare LLC

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar,…

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

Heytea USA Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2026

Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune…

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

Imu-Tek Animal Health, Incorporated

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved…

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

Intuitive Surgical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953

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

Jfe Franchising Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Drugs

Reported Apr 8, 2026

Sterile EYE DROPS AC (tetrahydrozoline HCl 0.05%, zinc sulfate 0.25%), 0.5 fl. oz. (15 mL) bottles; a) Best Choice,…

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

K.C. Pharmaceuticals, Inc.

7 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Apr 8, 2026

Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes

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

Lone Star Dairy Products LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

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

Medline Industries, LP

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

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

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height…

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

Mentor Texas, LP.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS…

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

Olympus Corporation of the Americas

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem

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

Oxoid Australia Pty Limited

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Allura Xper FD10C; System Code: 722001;

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

Philips Medical Systems Nederland B.v.

22 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

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

Philips Respironics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ

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

Pocas International Corp.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number:…

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

ReCor Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

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

Reflexion Medical, Inc.

FDA (openFDA device enforcement)

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