Complete FDA and NHTSA recall records dated in 2018, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
The patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time.
PureFlow B Solution smaller chamber of the two chamber bag can burst electrolyte fluid and cause injury if it comes in contact with the eyes or skin
PureFlow B Solution smaller chamber of the two chamber bag can burst electrolyte fluid and cause injury if it comes in contact with the eyes or skin
Investigation of complaints of off taste color and taste found that the product contained 3 times the level of the primary ingredients than is specified in the product formulation.
Ingredient statement lists flour but does not declare wheat as a sub-ingredient.
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Product may be contaminated with Salmonella.
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
The product's ingredients statement does not indicate presence of coconut
Sweet Potato Rice is recalled due to a potential for contamination with Salmonella or Listeria monocytogenes.
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Pumpkin Pesto does not declare walnuts as ingredient or allergen.
California Department of Food and Agriculture sampled and found Salmonella in cheese imported from Mexico.
Shirley s Cookie Company Inc. has initiated a recall of the following product: Chocolate Peanut Butter Whoopie Pies 16 oz (454g)/ 4 4 oz that were labeled with Chocolate Whoopie Pies which…
Product contains unintentional presence of milk and therefore milk was not listed on the label as an ingredient.
Failed Impurities/Degradation Specifications; out of specification results observed for other individual impurities
Presence of Foreign Substance; metal shard found in tablet
CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodiethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of…
Failed Stability Specification: out of specification for iron content.
Cross contamination with other products: Product is being recalled due to the potential presence of unrelated ingredients (Benazepril, Haloperidol and Perphenazine).
After running the calibration curve, the recovery of the IgM kit control results decrease demonstrating a reduction in accuracy within the same day; control results may be out of range one…
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
A software issue may cause the liquid volume detection entries for 2nd and 3rd reagent bottles to be overwritten with the data from the 1st reagent bottle. Tosoh has released software…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
