FoodMar 22, 2017
Sea Port Products Frozen Raw Bay Scallops, packaged in a clear 5 lbs recall — FDA F-1618-2017
Frozen Raw Bay scallops are recalled due to a potential contamination with hepatitis A virus.
Class IFDA: TerminatedSea Port Products Corp
Latest records
Latest recalls — page 1680
The newest recall records with useful source details are listed here.
FoodMar 22, 2017
Sweets & Desserts Tres Leches Chocolate recall — FDA F-1604-2017
Undeclared food color: Yellow #5 and Yellow #5 lake, and Yellow #6 and Yellow #6 lake
Class IIFDA: TerminatedSweets & Desserts, Inc.
FoodMar 22, 2017
Oriental Packing Co Hot/Spicy Curry Powder recall — FDA F-1614-2017
Product samples tested positive for lead. Finished curry products tested and ground turmeric ingredient used to manufacture the curry seasoning also tested positive for lead.
Class IFDA: TerminatedOriental Packing Co., Inc.
FoodMar 22, 2017
GOULIBEUR containing small pure butter shortbreads Net weight 4.23 oz recall — FDA F-1587-2017
This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food…
Class IIFDA: TerminatedGOULIBEUR
FoodMar 22, 2017
Sweets & Desserts Cheesecake Parcha recall — FDA F-1602-2017
Undeclared Milk Undeclared food color: Red #40, Yellow #5, and Yellow #6 Undeclared Aspartame
Class IIFDA: TerminatedSweets & Desserts, Inc.
FoodMar 22, 2017
krispy kreme doughnut 2 count boxes recall — FDA F-1609-2017
Product may contain foreign matter, metal pieces.
Class IIFDA: Terminatedkrispy kreme doughnut corporation
FoodMar 22, 2017
J M Exotic Foods Ground Turmeric packaged as follows: a) FOOD LOCKER recall — FDA F-1613-2017
The firm received a notice from their supplier that a sample of ground turmeric was tested and found to have elevated levels of lead.
Class IFDA: TerminatedJ M Exotic Foods Inc.
DrugMar 22, 2017
Synergy Rx TCA PEEL SOLUTION in all strengths including: 5%, 10%, 15%, 18%, and 20%, TCA recall — FDA D-0573-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx RETINOIC ACID SOLUTION in all strengths including 0.3%, 0.4%, 0.5%, 1%, RETINOIC recall — FDA D-0542-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx ADAPALENE 0.1%, BENZOYL PEROXIDE 2.5% GEL, ADAPELENE 0.3%, BENZOYL PEROXIDE 2,5% recall — FDA D-0530-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx RETINOIC ACID all strengths including 0.025%, 0.05% and 0.1% CREAM, RETINOIC ACID recall — FDA D-0541-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx SUPREME CREAM recall — FDA D-0572-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx LIDOCAINE CREAM in all strengths including: 5%, 8%, 23%, 30%, LIDOCAINE / recall — FDA D-0593-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx MINOXADIL all strength including 2%, 5% and MINOXIDIL / RETINOIC ACID 5% / 0.025 recall — FDA D-0528-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx GLYCOLIC ACID SOLUTION, all strengths including 10%, 20%, 30%, 50%, and 60% recall — FDA D-0540-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx BL 20%/4% CREAM, BLT 20%/6%/4% CREAM, BLT 20%/6%/6%, BLT 20% 8% 4% CREAM, BLT 20% recall — FDA D-0532-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx MALEK'S MAGIC PLUS recall — FDA D-0564-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx CLINDAMYCIN 1%, AZELAIC ACID 10% CREAM, CLINDAMYCIN 1.2%/ TRETINOIN 0.05% GEL recall — FDA D-0534-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx BRIGHTENING CREAM recall — FDA D-0551-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx ACNE SOLUTION recall — FDA D-0550-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx SALICYLIC ACID SOLUTION in all strengths including 20%, 25%, 30%, and 40% recall — FDA D-0543-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx GLYCOLIC ACID 15% LOTION, GLYCOLIC ACID 20% GEL, GLYCOLIC ACID 6% LOTION recall — FDA D-0539-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
Synergy Rx VI PEEL recall — FDA D-0578-2017
Lack of Assurance of Sterility: There are also CGMP Deviations.
Class IIFDA: TerminatedSynergy Rx
DrugMar 22, 2017
PreviDent 5000 ppm, DRY MOUTH, 1.1% Sodium Fluoride, PRESCRIPTION STRENGTH TOOTHPASTE, SLS recall — FDA D-0521-2017
Label Mix up; rear panel is incorrectly labeled with the PreviDent 5000 Enamel Protect rear panel.
Class IIIFDA: TerminatedColgate Palmolive Co
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