95,018 total recalls in our database
Boston Scientific
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
Boston Scientific
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
Their is a potential that implanted pulse generators may stop delivering therapy due to an internal component issue.
Karl Storz Endoscopy
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Karl Storz Endoscopy
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
MEDLINE INDUSTRIES, LP - Northfield
Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of EN 14683.
Murata Vios
During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central Station Monitor (CSM) in the patient tiles view and is not seen at any other point during patient monitoring & not on the Bedside Monitor.
Their is a potential that implanted pulse generators may stop delivering therapy due to an internal component issue.
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
Unknown Manufacturer
The handheld hair dryers lack an immersion protection device, posing an electrocution or shock hazard to consumers, if the hair dryers fall into water when plugged in. The CPSC has determined that hair dryers not equipped with the integral immersion protection present a substantial product hazard.
Unknown Manufacturer
The recalled stadium seats have bleacher security hooks that can crack and break, posing fall and injury hazards to consumers.
Cabinet Health Inc., of Washington, D.C.
The plastic lid's closure can degrade after repeated openings, causing the lid's child-resistance to diminish, posing a risk of poisoning, if the contents are swallowed by young children.
Unknown Manufacturer
The recalled children's pajamas violate the flammability regulations for children's sleepwear, posing a risk of burn injuries to children.
Unknown Manufacturer
The recalled digital kitchen scales violate the mandatory federal regulations for consumer products containing button cell or coin batteries, because the scale has a lithium coin battery that can be easily accessed by children, and a spare coin battery provided with the product not in child resistant packaging, as required by Reese's Law. These violations pose an ingestion hazard. The recalled scales also do not have the required warnings. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
Unknown Manufacturer
The training cycles' adjustable seat can unexpectedly lower while in use, posing a fall hazard to the rider.
Pearhead, of Brooklyn, New York
Due to its size and shape, the wooden egg-shaped rattle in the recalled learning sets can get lodged in a child's throat, posing a choking hazard. This violates the federal regulations for infant rattles.
Undeclared yellow #5
Cal Yee Farm
Undeclared milk
Product contains undeclared milk and soy.
MR BING FOODS
Product may contain spoilage organisms.