Complete FDA and NHTSA recall records dated in 2014, 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.
This recall of LIPTRUZET is being initiated due to packaging defects. Some of the outer laminate foil pouches allowed in air and moisture, which could potentially decrease the effectiveness…
Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being conducted because the product was given 36 month expiration dates instead of the filed 24 months.
Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being conducted because the product was given 36 month expiration dates instead of the filed 24 months.
This recall of LIPTRUZET is being initiated due to packaging defects. Some of the outer laminate foil pouches allowed in air and moisture, which could potentially decrease the effectiveness…
Failed Dissolution Specifications: failure of dissolution test observed at nine month time point.
Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel capsules.
Losurdo Foods has recalled one lot of Grated Cheese Pecorino Romano due to Listeria monocytogenes contamination.
Basil, Asiago & Pine Nut Pesto Ravioli is labeled with the ingredient statement for Itsy Bitsy ravioli and therefore does not include Pine Nuts in the ingredient or allergen statement.
Schwans Food Company is recalling Cheddar Cheese Puffs and Gourmet Cold Canapes Assortment manufactured by Holiday Foods, Inc that were prepared with ingredients which are being recalled by…
Schwans Food Company is recalling Cheddar Cheese Puffs and Gourmet Cold Canapes Assortment manufactured by Holiday Foods, Inc that were prepared with ingredients which are being recalled by…
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device.
Labeling: Label Error on Declared Strength; Firm states that erroneous potency information was found on the label.
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Non-Sterility: Complaints of leaks and particulate matter identified as mold in the solution bag and the overpouch.
Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device.
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Failed Impurities/Degradation Specifications: Out of Specification for an impurity at the 18 month stability time point.
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve sample units.
Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.
Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor.
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.
