Turkeyfoot Creek Creamery Mocha Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
Turkeyfoot Creek Creamery
Undeclared allergen - soy
95,102 total recalls in our database
Turkeyfoot Creek Creamery
Undeclared allergen - soy
Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.
Undeclared allergens (Peanut) due to mispackaging
Turkeyfoot Creek Creamery
Undeclared allergens - soy and wheat
MING HONG INTERNATIONAL
Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5.
Undeclared allergens (Peanut) due to mispackaging
Sub-Potent Drug: Subpotent assay results during stability testing.
Mckesson Medical-Surgical Inc. Corporate Office
CGMP Deviations; potential temperature excursions due to transit delays
Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
Sub-Potent Drug: Subpotent assay results during stability testing.
Lupin Pharmaceuticals
Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry.
Mckesson Medical-Surgical Inc. Corporate Office
CGMP Deviations; potential temperature excursions due to transit delays
Mckesson Medical-Surgical Inc. Corporate Office
CGMP Deviations; potential temperature excursions due to transit delays
MEDLINE INDUSTRIES, LP - Northfield
Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's ability to cancel a high voltage therapy delivery.
Beckman Coulter
A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing falsely increased assay results for the impacted Estrone RIA kits.
MEDLINE INDUSTRIES, LP - Northfield
Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.
Olympus Corporation of the Americas
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Olympus Corporation of the Americas
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).