DrugJul 27, 2022
Nephron Sterile Compounding Center Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac recall — FDA D-1249-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 89
10,685 detailed records are currently available in this category.
DrugJul 27, 2022
Nephron Sterile Compounding Center 8.4% Sodium Bicarbonate Injection, USP, 4.2 g/50 mL recall — FDA D-1279-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Morphine Sulfate Injection, USP, 30 mg/30 mL (1 mg/mL) recall — FDA D-1266-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Ketamine HCl Injection, USP, 50 mg/5 mL (10 mg/mL*) recall — FDA D-1259-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Glycopyrrolate Injection, USP, 0.6 mg/3 mL (0.2 mg/mL) recall — FDA D-1254-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center HYDROmorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL) recall — FDA D-1256-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Neostigmine Methylsulfate Injection, USP, 4 mg/4 mL recall — FDA D-1271-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Fentanyl Citrate in 0.9% Sodium Chloride Injection, USP recall — FDA D-1252-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Phenylephrine HCl Injection, USP, 0.4 mg/10 mL recall — FDA D-1274-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Loud Muscle Science Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC recall — FDA D-1338-2022
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this…
Class IFDA: TerminatedLoud Muscle Science
DrugJul 27, 2022
Nephron Sterile Compounding Center Morphine Sulfate Injection, USP, 1 mg/mL syringe recall — FDA D-1268-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Loud Muscle Science Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN recall — FDA D-1336-2022
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this…
Class IFDA: TerminatedLoud Muscle Science
DrugJul 27, 2022
Loud Muscle Science Launch Sequence Euphoria Capsules, 10- count tins, ASIN B08ZJX4V9J, UPC recall — FDA D-1337-2022
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this…
Class IFDA: TerminatedLoud Muscle Science
DrugJul 27, 2022
Amazon.com Artri King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle recall — FDA D-1297-2022
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Class IFDA: TerminatedAmazon.com, Inc.
DrugJul 27, 2022
Nephron Sterile Compounding Center Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL) recall — FDA D-1262-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL) recall — FDA D-1276-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Difluprednate Ophthalmic Emulsion, 0.05%, 5ml bottles recall — FDA D-1283-2022
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
Class IIFDA: TerminatedCIPLA
DrugJul 27, 2022
Nephron Sterile Compounding Center Rocuronium Bromide Injection, 50 mg/5 mL (10 mg/mL) recall — FDA D-1277-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Ketamine HCl Injection, USP 30 mg/3 mL (10 mg/mL*) recall — FDA D-1260-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL recall — FDA D-1272-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Apotex Aripiprazole Tablets, USP 20 mg recall — FDA D-1285-2022
Failed dissolution specifications: OOS for dissolution at the 12-month stability time point.
Class IIFDA: TerminatedApotex Corp.
DrugJul 27, 2022
Nephron Sterile Compounding Center Morphine Sulfate Injection, USP, 2 mg/2 mL (1 mg/mL) recall — FDA D-1267-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center HYDROmorphone HCl Injection, USP 30 mg/30 mL (1 mg/mL) recall — FDA D-1257-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
DrugJul 27, 2022
Nephron Sterile Compounding Center Atropine Sulfate Injection, USP 1.2 mg/3 mL (0.4 mg/mL) recall — FDA D-1246-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedNephron Sterile Compounding Center LLC
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.