Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
All Recalls
92,900 total recalls in our database
Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.
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.
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.
Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE, REF DYNJ58648B; 2) ENDOSCOPIC SKULL BASE, REF DYNJ58648C; 3) ENT ENDO SINUS WILMINGTON PACK, REF DYNJ66447; 4) ENDOSCOPIC SKULL BASE, REF DYNJ58648D; 5) ENDOSCOPIC SKULL BASE, REF DYNJ58648J.
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.
See DocMan
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.
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
Medtronic Neuromodulation
Software issues were identified in application version 2.x.
See DocMan
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 custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
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.
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN TABLET PAPER EN with the A810 CP app version 2.x, CFN CT900E
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 custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK, REF DYNJ66449.
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.
Wemfg Children's Multi-Purpose Bike Helmets
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.
SIG SAUER ROMEO5 Red Dot Sights
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.
Euqee Wintergreen Essential Oils
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.
John Deere ZTrakβ’ Zero Turn Mowers with Kawasaki Engines
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.
Yaomiao Children's Jewelry Sets
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.