Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Baxter Healthcare
Devices were identified as released after repair without full testing being performed, which includes flow testing.
95,018 total recalls in our database
Baxter Healthcare
Devices were identified as released after repair without full testing being performed, which includes flow testing.
MEDLINE INDUSTRIES, LP - Northfield
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
MEDLINE INDUSTRIES, LP - Northfield
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Medtronic Neuromodulation
Software issues were identified in application version 2.x.
MEDLINE INDUSTRIES, LP - Northfield
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
MEDLINE INDUSTRIES, LP - Northfield
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Medtronic Neuromodulation
Software issues were identified in application version 2.x.
Due to an increase of complaints for bracket bond failures and skin irritation or blistering.
MEDLINE INDUSTRIES, LP - Northfield
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Unknown Manufacturer
The helmets do not comply with the positional stability, impact labeling and certification requirements in violation of the CPSC federal safety regulation for bicycle helmets. The helmets can fail to protect in the event of a crash, posing a risk of head injury.
Unknown Manufacturer
The recalled firearm sights contain a button cell battery that violates the mandatory federal regulations for consumer products containing button cell batteries because the button cell batteries can be easily accessed, posing an ingestion hazard. The products include a button cell battery which is not in child-resistant packaging as required by Reese's Law. In addition, the products do not bear the required warnings. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death, posing an ingestion hazard to children.
Unknown Manufacturer
The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
Kawasaki Motors Manufacturing Corp. U.S.A. (engine manufacturer), of Maryville, Missouri
The voltage regulator in the mower's engine can fail during use or while the product is being stored, causing the engine to overheat, posing fire and burn hazards.
Unknown Manufacturer
The recalled jewelry sets contain levels of lead that exceed the federal lead content ban and levels of cadmium that are prohibited in children's products by the Federal Hazardous Substances Act. Lead and cadmium are toxic if ingested by young children and can cause adverse health effects.
Product contains undeclared fish (anchovy) and soy.
Eggs from a positive Salmonella environment were shipped into distribution to retail facilities.
Potential for Salmonella
Cucumbers potentially contaminated with Salmonella.