Complete FDA and NHTSA recall records dated in 2019, 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 glass syringe used with Pressure Control Syringes may potentially break during use.
As a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result in lower…
As a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result in lower…
As a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result in lower…
The epoxy on Apex manufactured epoxy-coated instruments can pop off.
packaging error; An internal QA inspection revealed that a incorrect healing collar could have been packaged in an implant assembly kit.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
Firm received consumer complaint of an allergic reaction after consumption.
Positive for histamine level at 140 ppm.
Firm received consumer complaint of an allergic reaction after consumption.
Firm received consumer complaint of an allergic reaction after consumption.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
The Winter Citrus Slaw Kit, item #71909, is recalled due to a potential contamination of Listeria monocytogenes.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
Firm received consumer complaint of an allergic reaction after consumption.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
Canned salmon product was recalled because it may have been under-processed and firm can't find the lot code in their canning records.
Firm received consumer complaint of an allergic reaction after consumption.
Cream cheese frosting was put in a container labeled as Creamy Chocolate Frosting. The chocolate frosting label fails to declare the presence of the major food allergen Milk.
Firm received consumer complaint of an allergic reaction after consumption.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).
CGMP Deviations: Presence of NDMA impurity detected in product.
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.
