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Recall archive

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

32,364 recalls · page 17 of 1349

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Pooled Cryoprecipitated AHF

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

ImpactLife

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 6, 2026

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) ,…

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

Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Cardioroot Woven Collagen Coated Vascular Graft; Model Numbers: 1. HEWROOT0024, 2. HEWROOT0026, 3. HEWROOT0028, 4.…

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

Intervascular, Sas

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

Iowa Lions Eye Bank

FDA (weekly enforcement report)

Food

Reported Sep 30, 2026Updated Oct 6, 2026

American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET WT. 8 oz.

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

Kwok Shing, Inc.

FDA (openFDA food enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 17, 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)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Red Blood Cells, Leukocytes Reduced

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

LifeStream Blood Bank

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

Lions Eye Bank Of Nebraska

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 6, 2026

Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ,…

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

Macleods Pharmaceuticals Limited

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2.…

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

Maquet SAS

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 8, 2026

Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack…

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

Medline Industries, LP

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,…

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

Midmark Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Red Blood Cells, Leukocytes Reduced

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

Mississippi Blood Services Inc.

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 10, 2026

Apheresis Platelets, Leukocytes Reduced

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

New York Blood Center Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

New York Embroidery Studio Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large. Model Number: NYES100-2.…

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

New York Embroidery Studio, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm. Model Number: BD-420X-1355.

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

Olympus Corporation of the Americas

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated

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

OneBlood, Inc.

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

OneLegacy

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

0.9% Sodium Chloride Injection, 100 mL, USP, ICU Medical, Inc., Lake Forest, Illinois 60045, USA, NDC 0990-7984-23.

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

Otsuka ICU Medical LLC

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Red Blood Cells, Leukocytes Reduced

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

Penn State Health Holy Spirit Medical Center

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initial system; Model Numbers (REF): 1. 781196 (Achieva 1.5T),…

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

Philips North America LLC

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

Precision Ocular Network - Bartlett

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

Rocky Mountain Lions Eye Bank

FDA (weekly enforcement report)

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