Rich Ice Cream Co Cool Watermelon Bar recall — FDA H-0293-2025
Potential Listeria Monocytogenes Contamination
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Potential Listeria Monocytogenes Contamination
Foreign material (plastic pieces)
Listeria monocytogenes. The firm was notified by their supplier that the product is contaminated with Listeria monocytogenes.
Product does not declare allergen ingredient sesame.
Potential contamination with floating objects
Foreign material (plastic pieces)
Potential Listeria Monocytogenes Contamination
Foreign material (plastic pieces)
Subpotent Drug: Assay below the approved specification
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Subpotent Drug: Assay below the approved specification
Subpotent Drug: Assay below the approved specification
Subpotent Drug: Assay below the approved specification
Subpotent Drug: Assay below the approved specification
Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability station (25C, 60%RH).
Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue resulted in incorrect lot numbers on the label.
Subpotent Drug: Assay below the approved specification
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.
Subpotent Drug: Assay below the approved specification
Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet…
Chrysler (FCA US, LLC) is recalling certain 2023-2024 Jeep Grand Cherokee and Jeep Grand Cherokee L vehicles. The second-row seat head restraints may not lock in the upright position. As…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Browse recent months with enough recall history for useful comparison.