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Recall archive

94,390 stored notices, from Jun 20, 2012 to Sep 23, 2026.

31,892 recalls · page 94 of 1329

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

ADDitIV utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space…

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

B Braun Medical Inc.

115 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Drugs

Reported Dec 3, 2025

Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San…

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

CA BOTANA International, Inc.

13 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 3, 2025

Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.

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

Cepheid

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use…

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

Dermasensor Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

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

Djo, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

FoundationOne CDx (F1CDx), RAL-0003 version 31.0

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

Foundation Medicine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Face Rock Creamery Vampire Slayer Garlic Cheddar, net wt. 6oz. Ready to Eat, Refrigerated/ Perishable. Product is…

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

Frc Inc.

FDA (openFDA food enforcement)

Drugs

Reported Dec 3, 2025

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC…

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

Fresenius Kabi USA, LLC

FDA (openFDA drug enforcement)

Food

Reported Dec 3, 2025Updated Aug 26, 2026

Fromm Family Foods recalls Bonnihill Farms BeefiBowls Beef Recipe gently cooked frozen dog food, 16 oz. chubs due to Potential foreign plastic contamination

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

Fromm Family Foods

FDA (recalls & safety alerts)

Medical devices

Reported Dec 3, 2025

SJM Pericardial Patch, with EnCap Technology 9x14cm, Model Number REF C0914; PATCH, PLEDGET AND INTRACARDIAC, PETP,…

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

Glycar SA Pty., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

DEVI brand Cinnamon Powder (Dalchini Powder), net wt.: 3.5 oz (100 g), packaged in flexible plastic bag. UPC 6 09595…

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

Homeneeds Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

FlexLab (FLX); Version: FLX-217-10;

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

Inpeco S.A.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

IntelePACS - InteleConnect / TechPortal

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

Intelerad Medical Systems Incorporated

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton…

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood.…

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

Magellan Diagnostics, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 3, 2025

Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD.,…

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

Medical Products Laboratories, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding model numbers: 1. SPACER 6068073…

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

Medtronic Sofamor Danek USA Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775

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

MeriCal, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap.…

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

Mindray DS USA, Inc. dba Mindray North America

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.

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

Nats Nuts LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy…

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

Noah Medical Corporation

FDA (openFDA device enforcement)

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