May contain low levels of peanut residue.
All Recalls
95,094 total recalls in our database
Meduri Farms Dried Blueberries/Sugar Infused product is recalled due to a potential contamination with peanut protein. The firm found half of a peanut while packaging dried blueberries product.
Product was found to be contaminated with Salmonella. Product was distributed to food service established only.
IEH sample of Whole Foods Raw Macadamia nuts had a positive result for Salmonella.
Potential presence of Listeria Monocytogenes
Blueberry Cheesecake, 5 oz.
Spartan Stores
SpartanNash Company initiated a voluntary recall of Cherry, Strawberry, and Blueberry Cheesecakes with a sell by date of 06/06/2016 to 06/21/2016, due to the potential for undeclared allergen peanut residue resulting from a supplier's recall of graham cracker crumbs.
Potential presence of Listeria Monocytogenes
Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for injection, Rx Only, Isomeric Pharmacy Solution, 2401 Foothill Dr., Salt Lake City, UT 84109
Isomeric Pharmacy Solution
Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate 7 mg/mL INJ SUSP because of the potential of drug clumps in the vial of the sterile drug product and larger particle sizes.
Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to nasal decongestant claims as well as not complying with the nasal decongestant final monograph.
Failed Content Uniformity Specifications: out of specification test result for spray content uniformity.
Isolated episodes of leakage at the check valve were found
Beckman coulter has received complaints regarding leaking and cracked C cups. When the cup cracks, coolant can leak onto the connectors of the Printed Circuit Boards (PCB) in the analyzer, resulting in a short-circuit causing the instrument to go into a stop mode.
Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirschner Wire (K-Wire) component.
The manufacturing and expiration dates are not printed on the blister pack label.
Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug cup, because it may erroneously contain 12 panel cups due to a packaging error.
The surface coating applied to the device is blistering, peeling and discoloring after usage over time
Medtronic Navigation, Inc. announces a voluntary field action for the Medtronic Navigation StealthStation Software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.
The firm has received multiple reports of the Non-Invasive Blood Pressure (NIBP) parameter becoming non-functional with an associated message (No Reading). In addition, there is one of the following three error messages: Inflate Error, HW Error, or No Data.
Trigger lock option does not always prevent x-ray generation. Specifically if the unit is in test mode or repeat test mode then the trigger lock may not prevent x-ray initiation when the trigger is pulled. The correction is via repair by a software update.