FoodJan 15, 2014
Creole & Company NET WEIGHT 3.47 oz recall — FDA F-1645-2013
Product which contains milk, soy, and wheat was distributed without an ingredient statement which declares their presence.
Class IFDA: TerminatedCreole & Company, LLC
Monthly breakdown
2014 recalls by month
Select a month to review the recall records reported during that period.
December 2014206 records · 2 categoriesNovember 2014617 records · 2 categoriesOctober 2014159 records · 2 categoriesSeptember 2014101 records · 2 categoriesAugust 2014118 records · 2 categoriesJuly 2014224 records · 3 categoriesJune 201483 records · 2 categoriesMay 2014120 records · 2 categoriesApril 2014219 records · 2 categoriesMarch 2014137 records · 2 categoriesFebruary 2014124 records · 2 categoriesJanuary 20141,038 records · 2 categories
2014 recalls — page 117
Records are ordered by the best available source date.
FoodJan 15, 2014
Safeway Kitchens In Shell Edamame recall — FDA F-1383-2014
Product on hold pending FDA testing that found 0.015 ppm of the pesticide chlorafluazuron was inadvertently released to Safeway warehouses and a few retail stores.
Class IIIFDA: TerminatedSafeway Inc.
FoodJan 15, 2014
Innovative Labs Terrain Zyme Myco-Zyme recall — FDA F-1381-2014
Innovative Labs, LLC. has recalled two Dietary Supplements due to the presence of Chloramphenicol, an antimicrobial agent.
Class IIFDA: TerminatedInnovative Labs, LLC
FoodJan 15, 2014
Perrigo of SC EstroPlus Maximum Strength Menopause Support Dietary recall — FDA F-1384-2014
Potential presence of Chloramphenicol contamination
Class IIFDA: TerminatedPerrigo of SC
FoodJan 15, 2014
Del Monaco Specialty Foods Armanino Alfredo Sauce recall — FDA F-1385-2014
The product was not labeled with ingredients nor with an allergen declaration; the carton only contained one label which states the product identity by the second label with ingredients and…
Class IIFDA: TerminatedDel Monaco Specialty Foods Inc.
FoodJan 15, 2014
Innovative Labs Terrain Zyme LGS-Zyme recall — FDA F-1382-2014
Innovative Labs, LLC. has recalled two Dietary Supplements due to the presence of Chloramphenicol, an antimicrobial agent.
Class IIFDA: TerminatedInnovative Labs, LLC
FoodJan 15, 2014
Baugher Ranch Organics Organic Almonds: Baugher Ranch Organics recall — FDA F-1378-2014
Potential for metal fragments in product after a single wire from metal detector was confirmed to be cut into fragments and not all pieces are accounted for.
Class IIFDA: TerminatedBaugher Ranch Organics, Inc.
DrugJan 15, 2014
Mutual Pharmaceutical Company Fenofibric Acid, immediate release tablet, 35 mg, 30 count recall — FDA D-399-2014
Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed…
Class IIIFDA: TerminatedMutual Pharmaceutical Company, Inc.
DrugJan 15, 2014
Mutual Pharmaceutical Company FIBRICOR (fenofibric acid) Tablets, 105 mg, a) 30 count bottle recall — FDA D-398-2014
Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed…
Class IIIFDA: TerminatedMutual Pharmaceutical Company, Inc.
DrugJan 15, 2014
Compounding Centre At Blue Ridge Papaverine/Phentolamine 30 mg/mL/2.0 mg/mL Inj, 5 mL units recall — FDA D-405-2014
Lack of Assurance of Sterility; All lots of sterile products compounded by the pharmacy within expiry are subject to this recall. This recall is initiated due to concerns associated with…
Class IIFDA: TerminatedCompounding Centre At Blue Ridge
DrugJan 15, 2014
Compounding Centre At Blue Ridge Triple Mix Injectable recall — FDA D-401-2014
Lack of Assurance of Sterility; All lots of sterile products compounded by the pharmacy within expiry are subject to this recall. This recall is initiated due to concerns associated with…
Class IIFDA: TerminatedCompounding Centre At Blue Ridge
DrugJan 15, 2014
Mutual Pharmaceutical Company Fenofibric Acid, immediate release tablet, 105 mg, a) 30 count recall — FDA D-400-2014
Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed…
Class IIIFDA: TerminatedMutual Pharmaceutical Company, Inc.
DrugJan 15, 2014
Compounding Centre At Blue Ridge Super Triple Mix Injectable recall — FDA D-403-2014
Lack of Assurance of Sterility; All lots of sterile products compounded by the pharmacy within expiry are subject to this recall. This recall is initiated due to concerns associated with…
Class IIFDA: TerminatedCompounding Centre At Blue Ridge
DrugJan 15, 2014
Watson Laboratories Carisoprodol Tablets, USP, CIV, 350 mg, 500 count bottle recall — FDA D-397-2014
Presence of Foreign Substance; metal particulates were visually observed in the tablets.
Class IIFDA: TerminatedWatson Laboratories Inc.
DrugJan 15, 2014
Compounding Centre At Blue Ridge PGE 20 mcg/mL Injectable, 10 mL, and PGE 40 mcg/mL, 5 mL recall — FDA D-402-2014
Lack of Assurance of Sterility; All lots of sterile products compounded by the pharmacy within expiry are subject to this recall. This recall is initiated due to concerns associated with…
Class IIFDA: TerminatedCompounding Centre At Blue Ridge
DrugJan 15, 2014
Compounding Centre At Blue Ridge Quad Mix Injectable, 5 mL recall — FDA D-404-2014
Lack of Assurance of Sterility; All lots of sterile products compounded by the pharmacy within expiry are subject to this recall. This recall is initiated due to concerns associated with…
Class IIFDA: TerminatedCompounding Centre At Blue Ridge
FoodJan 8, 2014
Mira Health Products Biogenix USA Methadrol capsules, packaged in plastic bottles recall — FDA F-1333-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
FoodJan 8, 2014
Mira Health Products Biogenix USA HAM capsules, packaged as a bulk product in clear recall — FDA F-1329-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
FoodJan 8, 2014
Mira Health Products Nature Science Equibolix capsules, packaged as a bulk product recall — FDA F-1260-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
FoodJan 8, 2014
Atlantic Pro Nutrients, Inc. dba XYMOGEN XYMOGEN LipiChol recall — FDA F-0815-2014
Product was labeled as a medical food as opposed to a dietary supplement.
Class IIIFDA: TerminatedAtlantic Pro Nutrients, Inc. dba XYMOGEN
FoodJan 8, 2014
Mira Health Products Nature Science ADT capsules, packaged as a bulk product in recall — FDA F-1261-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
FoodJan 8, 2014
Mira Health Products Park Labs Vinicol capsules packaged in a plastic bottle with recall — FDA F-1302-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
FoodJan 8, 2014
Mira Health Products Nature Science Dym-Sdrol capsules, packaged as a bulk product recall — FDA F-1256-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
FoodJan 8, 2014
Mira Health Products B Complex, labeled in part as "Healthy Life Chemistry" By recall — FDA F-1289-2014
The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.
Class IIFDA: TerminatedMira Health Products Ltd.
About the 2014 recall archive
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.