Complete FDA and NHTSA recall records dated in December 2014.
These records include useful source details for the selected month.
Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.
Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.
Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.
Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products.
The product has the potential to be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
Mislabeling. Product inside a plastic bag actually contains milk but mis-labeled as "Everything Bagels" and this label does not declare milk.
The product has the potential to be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products.
The product has the potential to be contaminated with Listeria monocytogenes.
Product may contain mold.
The product has the potential to be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
The product has the potential to be contaminated with Listeria monocytogenes.
Failed Tablet/Capsule Specifications: Product being recalled due to the potential presence of cracked or broken capsules.
Lack of Assurance of Sterility; improperly crimped fliptop vials
Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
Presence of Particulate Matter: Baxter Healthcare Corporation has received a complaint reporting the presence of particulate matter identified as plastic/rubber in famotidine Injection…
Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
