Devices inappropriately displayed a low battery indicator determined to be due to memory corruption.
All Recalls
95,038 total recalls in our database
Potential for unsealed pouches in two (2) lots of the Endosee Advance Cannula (P/N: ESPX5).
CARESCAPE Respiratory Module E-sCAiOVE
GE Healthcare
Displayed End Tidal Oxygen (EtO2) and Fraction of Inspired Oxygen (FiO2) values may be incorrect which could cause up to 50% measurement error in the EtO2/FiO2 values.
Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500
Teleflex Medical
The device label incorrectly states that the device is sterile. This product is an externally applied male condom-type catheter designed for the management of male incontinence as an alternative to incontinence pads. In normal use, the device is neither expected nor required to be sterile.
Carestream Health has discovered a potential safety problem that can lead to unintended movement of the U-Arm.
The Bravo Mini (Model 250D), Agilis Mini (Model 250D), and NBP One (Model 250D) are being recalled because of a user safety issue when rechargeable batteries are misused in the product.
CARESCAPE Respiratory Module E-sCAiOE
GE Healthcare
Displayed End Tidal Oxygen (EtO2) and Fraction of Inspired Oxygen (FiO2) values may be incorrect which could cause up to 50% measurement error in the EtO2/FiO2 values.
CARESCAPE Respiratory Module E-sCO
GE Healthcare
Displayed End Tidal Oxygen (EtO2) and Fraction of Inspired Oxygen (FiO2) values may be incorrect which could cause up to 50% measurement error in the EtO2/FiO2 values.
CARESCAPE Respiratory Module E-sCOVX
GE Healthcare
Displayed End Tidal Oxygen (EtO2) and Fraction of Inspired Oxygen (FiO2) values may be incorrect which could cause up to 50% measurement error in the EtO2/FiO2 values.
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Howmedica Osteonics
May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire
Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx. The firm name on the label is Riverpoint Medical, LLC, Portland, OR.
Riverpoint Medical
The integrity of the sterile grid packaging is potentially compromised.
Teleflex MEDICAL RuSCH One piece Male External Medium Catheter W/O Tape, REF A1500M
Teleflex Medical
The device label incorrectly states that the device is sterile. This product is an externally applied male condom-type catheter designed for the management of male incontinence as an alternative to incontinence pads. In normal use, the device is neither expected nor required to be sterile.
Tango Mini Strollers
Baby Trend, of Fontana, Calif.
Both of the stroller's hinge joints can release and collapse under pressure, posing a fall hazard to children in the stroller.
The product contains undeclared sulfites.
Nestle Toll House Oatmeal Raisin Cookie Bar (16.5oz), UPC 050000062195
Gerber Products Company
Potential presence of food-grade rubber pieces.
Nestle Toll House Peanut Butter Chocolate Chip Bar (16oz), UPC 050000622634
Gerber Products Company
Potential presence of food-grade rubber pieces.
Nestle Toll House Fall'n Leaves Cookie Dough (16oz), UPC 050000415083
Gerber Products Company
Potential presence of food-grade rubber pieces.
Nestle Toll House Sugar Cookie Bar (16.5oz), UPC 050000622443
Gerber Products Company
Potential presence of food-grade rubber pieces.
M&M's Everyday Cookie Dough (14oz), UPC 050000417353
Gerber Products Company
Potential presence of food-grade rubber pieces.
Simply Fresh brand MiniMeals2Go Avocado Toast (6.75 OZ) ready-to-eat snack packs
Five Star Gourmet Foods of Florida
Products have potential to be contaminated with Listeria monocytogenes.