DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 MAGnesium 4gm in NS 100 mL (MAGnesium SULfate recall — FDA D-0936-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
10,690drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 206
10,690 detailed records are currently available in this category.
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 HEPARIN 1,000 Units in NS 250mL recall — FDA D-0948-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 fentaNYL 2 mcg/mL, 0.125% ROPivacaine, Fentanyl recall — FDA D-0946-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 NORepiNEPHrine 16 recall — FDA D-0958-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 0.2% ROPivacaine - OnQ Pump, (ROPivacaine HCL recall — FDA D-0928-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 ePHEDrine 50mg, 50 mg/10 mL (5 mg per mL) recall — FDA D-0930-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 NORepiNEPHrine4mg recall — FDA D-0960-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 Midazolam 1 mg/mL (Midazolam HCL recall — FDA D-0957-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 25, 2018
Metformin Hydrochloride Extended Release Tablets, USP, 500 mg recall — FDA D-0924-2018
Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in…
Class IIFDA: TerminatedSun Pharmaceutical Industries, Inc.
DrugJul 25, 2018
Avella of Deer Valley, Inc. Store 38 Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL recall — FDA D-0941-2018
Lack of Assurance of Sterility: Potential leakage of bags.
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugJul 18, 2018
SCA Pharmaceuticals Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local recall — FDA D-0918-2018
Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.
Class IIFDA: TerminatedSCA Pharmaceuticals
DrugJul 18, 2018
AMERICAN HEALTH PACKAGING Enalapril Maleate Tablets USP, 5 mg, 100 Tablets (10X10) blister recall — FDA D-0915-2018
Failed Impurities/Degradation Specification; out-of-specification results for the Enalapril DKT degradant
Class IIIFDA: TerminatedAMERICAN HEALTH PACKAGING
DrugJul 18, 2018
Piperacillin and Tazobactam for Injection USP 3.375 grams per vial, Single-Dose Vial recall — FDA D-1030-2018
Presence of Particulate Matter: identified as glass and silicone material
Class IFDA: TerminatedAuroMedics Pharma LLC
DrugJul 18, 2018
Medgyn Products Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single recall — FDA D-0917-2018
CGMP Deviations: The manufacturer of this product recalled because they were not manufactured under current good manufacturing practices.
Class IIFDA: TerminatedMedgyn Products, Inc.
DrugJul 18, 2018
Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection recall — FDA D-0925-2018
Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.
Class IIFDA: OngoingSanofi-Aventis U.S. LLC
DrugJul 18, 2018
Fluocinolone Acetonide Topical Solution, USP, 0.01%, 60 mL bottle recall — FDA D-0909-2018
Failed Impurities and Degradation Specifications and Subpotent Drug: out-of-specification (OOS) test results for below assay and above specification for degradants.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugJul 18, 2018
Medi-Fare Drug and Home Health Center Potassium Chloride For Injection Concentrate syringe recall — FDA D-0919-2018
CGMP Deviations: Syringes were filled with 19mL of potassium chloride when the labels displayed a fill of 20mL.
Class IIFDA: TerminatedMedi-Fare Drug and Home Health Center
DrugJul 18, 2018
Gaia Kratom (mitragyna speciosa) powder, Red Bali, 1oz, 250g, 1kg packages, Gaia recall — FDA D-1005-2018
Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination
Class IFDA: TerminatedGaia Ethnobotanical LLC
DrugJul 11, 2018
eb5 Skincare that Works recall — FDA D-0908-2018
Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity
Class IIFDA: TerminatedEb5 Corporation
DrugJul 11, 2018
LUPIN SOMERSET Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic recall — FDA D-0907-2018
Labeling: Not Elsewhere Classified - A private label distributor noted unfiled NDC numbers on EQ ClearLax Polyethylene Glycol 3350 NF Powder Solution of various sizes.
Class IIIFDA: TerminatedLUPIN SOMERSET
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
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 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
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…
How to use this drug recall index
A drug recall record can include the reason for recall, firm, status, distribution pattern, quantity and FDA classification. This site does not provide medical advice; it organizes public recall information and links users back to official sources.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
What the database can and cannot tell you
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.