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Recall archive

94,898 stored notices, from Jun 20, 2012 to Oct 14, 2026.

32,154 recalls · page 445 of 1340

Medical devices

Reported Apr 13, 2022

Excelsior Medical 10mL Sterile Field Saline Flush ZR, 0.9% Sodium Chloride Injection, USP, REF EMZ10091280, Sterile, IV…

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

MEDLINE INDUSTRIES, LP - Northfield

FDA (openFDA device enforcement)

Drugs

Reported Apr 13, 2022

Janumet (sitagliptin and metformin HCl) tablets, 50 mg/500 mg, 14-count bottle, packaged as 2 bottles per carton ,…

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

Merck Sharp & Dohme Corp.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 13, 2022

Travoprost Ophthalmic Solution, USP, 0.004%, 2.5 mL bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc.,…

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

Mylan Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Apr 13, 2022

Accuretic (quinapril HCl/hydrochlorothiazide) Tablets, 10 mg/12.5 mg*, 90 Tablets bottles, Rx Only, Distributed by:…

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

Pfizer Inc.

7 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 13, 2022

Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x

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

Philips Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

Philips Allura (Model Numbers 722010, 722012, 722026, 722027, 722028, 722029, 722035) and Philips Azurion (Model…

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

Philips North America LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Drugs

Reported Apr 13, 2022

The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint, 16.9 FL OZ (500 mL, Manufactured for Revive Personal…

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

Revive Personal Products Company

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 13, 2022

Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm

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

Sa3, LLC

FDA (openFDA device enforcement)

Drugs

Reported Apr 13, 2022

Orphenadrine Citrate Extended-Release Tablets, USP 100 mg, Rx Only, 100 Tablets, Manufactured by Sandoz Inc.,…

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

Sandoz, Inc.

FDA (openFDA drug enforcement)

Food

Reported Apr 13, 2022

Caesar dressing in a 1.5 oz pouch

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

Sauer Brands Inc. - New Century

FDA (openFDA food enforcement)

Medical devices

Reported Apr 13, 2022

MODEL: X-RAY R/F SYSTEM FLUOROspeed X1

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

Shimadzu Medical Systems

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

YSIO X.Pree

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

Surgicare Neuro Pack - Neurological Kit

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

Stradis Medical, LLC dba Stradis Healthcare

4 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Apr 13, 2022

Cequa (cyclosporine ophthalmic solution) 0.09%, packaged in 6 pouches x 10 single-use vials (0.25 mL each) per box,…

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

Sun Pharmaceutical Industries Inc.

FDA (openFDA drug enforcement)

Food

Reported Apr 13, 2022

Yes! Enoki Mushrooms; Pesticide Free Produce: Vacuumed packed. Product of China 5.29 oz. (150g) packaged in pink and…

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

T Fresh Company dba Yes Produce

FDA (openFDA food enforcement)

Food

Reported Apr 13, 2022

Thai Noodle Salad Kit 108 oz. bag (behind the counter salad), UPC 0 30223 11270 9, Taylor Farms Southwest, 859 S. 86th…

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

Taylor Farms Southwest, Inc.

FDA (openFDA food enforcement)

Drugs

Reported Apr 13, 2022

23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx Only, RITEDOSE, 503B…

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

The Ritedose Corporation

FDA (openFDA drug enforcement)

Food

Reported Apr 13, 2022

Top Quality Produce Enoki Mushrooms; 200G/7.05 oz. clear package with green bottom. Vacuumed packed Product of Taiwan.…

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

Top Quality Produce, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 13, 2022

BenchMark ULTRA and DISCOVERY ULTRA Instruments

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

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Drugs

Reported Apr 13, 2022

TETRACAINE 1% Tetracaine HCI Injection, USP, 20mg/2mL (10mg/mL), 10 x 2ml Single Use Vials per box, Rx only,…

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

Vitae Enim Vitae Scientific, Inc.

3 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 13, 2022

SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x

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

Volcano Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

First SIGN SARS-CoV-2 Antigen Test

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

WHPM Inc.

FDA (openFDA device enforcement)

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