FoodApr 13, 2016
Bj Wholesale Club Kunzler Sweet Bologna, sold in a deli bag recall — FDA F-0962-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
April 2016 recalls — page 7
These records include useful source details for the selected month.
FoodApr 13, 2016
Bj Wholesale Club D&W BBQ CHICKEN, packaged in deli bag recall — FDA F-0933-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Bj Wholesale Club D&W BUFFALO CHICKEN, packaged in deli bag recall — FDA F-0938-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Bj Wholesale Club WF Sandwich Ring substitute Roast Beef recall — FDA F-0979-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Bj Wholesale Club D&W Black Forest Turkey, packaged in deli bag recall — FDA F-0935-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Bj Wholesale Club CITTERIO CHORIZO, sold in a deli bag recall — FDA F-0992-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Pacific Coast Fruit Company VA Kit Roasting Brussel Sprouts, Item #72893 recall — FDA F-1025-2016
VA Kit Roasting Brussel Sprouts, Item #72893, is recalled due to a possible exposure to walnut.
Class IFDA: TerminatedPacific Coast Fruit Company
FoodApr 13, 2016
Bj Wholesale Club D&W Black Pepper Turkey, packaged in deli bag recall — FDA F-0936-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Bj Wholesale Club DAK HAM, sold in a deli bag recall — FDA F-0952-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Bj Wholesale Club APPLEGATE HAM BLACK FOREST, packaged in deli bag recall — FDA F-0927-2016
Product may have been sliced on the same equipment where the mortadella with pistachios was sliced.
Class IIFDA: TerminatedBj Wholesale Club
FoodApr 13, 2016
Immuno - Dynamics Colostrum Powder, Dietary Supplement, Allergen statement recall — FDA F-1013-2016
The PerCoBa brand and Synertek brand Colostrum product labels should state contains milk.
Class IIIFDA: TerminatedImmuno - Dynamics, Inc.
FoodApr 13, 2016
Yummy Earth YumEarth Organics Gummy Worms Net Wt recall — FDA F-1022-2016
Gummy Worms and Gummy Bears are labeled incorrectly in that the outer package lists 11 mg carbohydrates and the individual packages lists 18 mg carbohydrates.
Class IIFDA: TerminatedYummy Earth Inc.
FoodApr 13, 2016
Abbott Nutrition The product is labeled as follows: PediaSure Grow & Gain recall — FDA F-1041-2016
Abbott Nutrition is recalling PediaSure Grow & Gain Vanilla is product because the product may have a different color, smell, taste or texture inconsistent with other lots of PediaSure…
Class IIFDA: TerminatedAbbott Nutrition
DrugApr 13, 2016
Meditech Laboratories Formula 2 recall — FDA D-0808-2016
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 2 recall — FDA D-0802-2016
Superpotent Drug: one ingredient was found to be above assay specification.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Apace KY Minocycline Hydrochloride Capsules USP, 100 mg*, 30 Capsules (3 x 10) Unit Dose recall — FDA D-0811-2016
Labeling: Incorrect or Missing Lot and/or Exp Date: the individual blisters are mislabeled with an incorrect lot number of 13560 rather than the correct lot number of 13650.
Class IIIFDA: TerminatedApace KY LLC
DrugApr 13, 2016
Meditech Laboratories Formula 1 recall — FDA D-0805-2016
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Meditech Laboratories Formula 3 recall — FDA D-0806-2016
Stability Does Not Support Expiry: manufactured with an active ingredient that expired before the labeled Beyond Use Date.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Bio-pharm Ranitidine Syrup recall — FDA D-0809-2016
Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.
Class IIIFDA: TerminatedBio-pharm, Inc.
DrugApr 13, 2016
Actavis Elizabeth Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine recall — FDA D-0815-2016
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Class IIFDA: TerminatedActavis Elizabeth LLC
DrugApr 13, 2016
Virtus Pharmaceuticals VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing recall — FDA D-0801-2016
Defective Delivery System: Product may contain leaking capsules.
Class IIIFDA: TerminatedVirtus Pharmaceuticals, LLC
DrugApr 13, 2016
Meditech Laboratories Formula 9 recall — FDA D-0804-2016
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
DrugApr 13, 2016
Actavis Elizabeth Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine recall — FDA D-0814-2016
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Class IIFDA: TerminatedActavis Elizabeth LLC
DrugApr 13, 2016
Meditech Laboratories Formula 4 recall — FDA D-0803-2016
Lack of Assurance of Sterility: incomplete or missing data regarding production.
Class IIFDA: TerminatedMeditech Laboratories, Inc.
How to use this monthly recall archive
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.