FoodJul 11, 2018
Caito Foods Service Multiple Brands Mixed Melon: Customer Product Description Pack recall — FDA F-1631-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
Latest records
Latest recalls — page 1406
The newest recall records with useful source details are listed here.
FoodJul 11, 2018
Caito Foods Service Cantaloupe, multiple product sizes and brands, see as follows recall — FDA F-1624-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
FoodJul 11, 2018
Caito Foods Service Multiple Brands Mixed Melon: Customer Product Description Pack recall — FDA F-1632-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
FoodJul 11, 2018
SNI Nitric Blast Sour Apple 276gr recall — FDA F-1604-2018
SNI, LLC is recalling certain Nitric Blast brand products that contain geranium extract as a dietary ingredient. This ingredient is also called, among other names, dimethylamylamine,…
Class IIFDA: TerminatedSni LLC
FoodJul 11, 2018
Caito Foods Service WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386 recall — FDA F-1623-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
FoodJul 11, 2018
Caito Foods Service Multiple Brands Mixed Melon: Customer Product Description Pack recall — FDA F-1634-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
FoodJul 11, 2018
Caito Foods Service Multiple Brands Mixed Melon: Customer Product Description Pack recall — FDA F-1642-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
FoodJul 11, 2018
Caito Foods Service Multiple Brands Mixed Melon: Customer Product Description Pack recall — FDA F-1633-2018
Products have the potential to be contaminated with Salmonella.
Class IFDA: TerminatedCaito Foods Service, Inc.
DrugJul 11, 2018
SCA Pharmaceuticals Phenylephrine HCL 80mg in 0.9% Sodium Chloride 250 mL Bag (320 mcg/mL) recall — FDA D-0905-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial recall — FDA D-0891-2018
Superpotent Drug: High out of specification assay value results for potency.
Class IIFDA: TerminatedIngenus Pharmaceuticals LLC
DrugJul 11, 2018
SCA Pharmaceuticals Phenylephrine HCL 40 mg in 0.9% Sodium Chloride 250 mL Bag (160 mcg/mL) recall — FDA D-0902-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
Fagron Compounding Services LLC dba Fagron Neostigmine Methylsulfate Injection Solution, 3 recall — FDA D-0911-2018
Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3…
Class IFDA: TerminatedFagron Compounding Services LLC dba Fagron Sterile…
DrugJul 11, 2018
SCA Pharmaceuticals Fentanyl (as citrate) 2 mcg/mL + Bupivacaine HCL 0.0625% in 0.9% Sodium recall — FDA D-0896-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial recall — FDA D-0890-2018
Superpotent Drug: High out of specification assay value results for potency.
Class IIFDA: TerminatedIngenus Pharmaceuticals LLC
DrugJul 11, 2018
SCA Pharmaceuticals Phenylephrine HCL 50 mg in 0.9% Sodium Chloride 250 mL Bag (200 mcg/mL) recall — FDA D-0904-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Norepinephrine Bitartrate 16 mg (64 mcg/mL) in 0.9% Sodium Chloride 250 recall — FDA D-0900-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Norepinephrine Bitartrate 4 mg (16 mcg/mL) in 0.9% Sodium Chloride 250 recall — FDA D-0898-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Fentanyl (as citrate) 10 mcg/mL in 0.9% Sodium Chloride 250 mL bag, SCA recall — FDA D-0895-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Morphine Sulfate 1 mg/mL recall — FDA D-0894-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Phenylephrine HCL 20 mg in 0.9% Sodium Chloride 250 mL Bag (160 mcg/mL) recall — FDA D-0903-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
Fagron Compounding Services LLC dba Fagron Neostigmine Methylsulfate Injection Solution, 5 recall — FDA D-0910-2018
Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3…
Class IFDA: TerminatedFagron Compounding Services LLC dba Fagron Sterile…
DrugJul 11, 2018
SCA Pharmaceuticals Phenylephrine HCL 10 mg in 0.9% Sodium Chloride 250 mL Bag (40 mcg/mL) recall — FDA D-0901-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Diltiazem HCL 1 mg/mL in 125 mL 0.9% Sodium Chloride 100 mL bag recall — FDA D-0897-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
DrugJul 11, 2018
SCA Pharmaceuticals Norepinephrine Bitartrate 8 mg (32 mcg/mL) in 0.9% Sodium Chloride 250 recall — FDA D-0899-2018
Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.
Class IIFDA: TerminatedSCA Pharmaceuticals, LLC
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Recent recall archives
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October 2026244 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories