🔍 RecallPedia

All Recalls

95,114 total recalls in our database

🍎
28,983
Food
 💊
17,685
Drugs
 🏥
38,779
Medical Devices
 🏠
9,667
Consumer Products

YOUNG DH Dry Heat Indicators, PRESSURE SENSITIVE LABELS with COLOR INDICATOR STRIP, REF 116312 Intended for use by a health care provider to accompany products being sterilized through a sterilization procedure and to monitor one or more parameters of the sterilization process.

Young Dental Mfg Co I

🏥 Medical Devices Class I - Dangerous

The Dry Heat Indicator Labels packaging may contain TTS Indicator Labels instead of Dry Heat Indicator Labels.

Dec 29, 2021 Diagnostic Equipment View Details →

ARIES HSV 1&2 Assay, Catalog/REF# 50-10017

Luminex

🏥 Medical Devices Class I - Dangerous

Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak rate of 0.9%. Leaking cassettes could potentially lead to incorrect results or a delay in reporting results due to an Invalid.

Nov 17, 2021 Other Medical Devices Nationwide View Details →

The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length varying from 16 mm to 80.5 mm according to the electrode reference. Microdeep Depth Electrodes are intended for temporary use with recording, monitoring and stimulation equipment for the recording, monitoring and stimulation of electrical signals at the subsurface level of the brain.

DIXI MEDICAL USA

🏥 Medical Devices Class I - Dangerous

Potential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag

Dec 9, 2021 Diagnostic Equipment Nationwide View Details →

Premier Rotaclone, Rx only

MEDLINE INDUSTRIES, LP - Northfield

🏥 Medical Devices Class I - Dangerous

Product stored incorrectly in temperature controlled setting instead of refrigeration.

Dec 1, 2021 Other Medical Devices Nationwide View Details →

OXY-1 System, Model Number 001-0500-001. Used during cardiopulmonary bypass. OXY-1 System consists of Console, Pump Drive, E Drive, and Pole Mount. The disposable Pump Lung Unit PLU part number 001-0400-100 is sold separately and is not part of this recall.

Abiomed

🏥 Medical Devices Class I - Dangerous

The firm has received complaints of the OXY-1 System Console experiencing a power interruption while in use, which disrupts therapy delivered to a patient on support. Disruption of therapy could lead to prolonged hypoxia.

Dec 14, 2021 Infusion Pumps View Details →

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product code 35700BAX2.

Baxter Healthcare

🏥 Medical Devices Class I - Dangerous

There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms when using Spectrum V8 and Spectrum IQ infusion pumps.

Dec 29, 2021 Infusion Pumps Nationwide View Details →

Children's Nightgowns

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

The children's nightgowns fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.

Feb 9, 2022 Children's Products Nationwide View Details →

Personal Electric Heaters

Unknown Manufacturer

🏠 Consumer Products Class I - Dangerous

The toggle power switch can spark when the switch is used, posing a fire hazard.

Feb 9, 2022 Home & Garden Nationwide View Details →

Adam the Apple™ Children's Stackable Toys

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

Surface paint on the wooden toys contains levels of lead that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health effects.

Feb 9, 2022 Children's Products Nationwide View Details →

River Street Five-Drawer Chests

Unknown Manufacturer

🏠 Consumer Products Class I - Dangerous

The recalled dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children. The dressers do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM 2057-19).

Feb 3, 2022 Other Consumer Products Nationwide View Details →