DrugOct 7, 2015
Medistat RX All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave. recall — FDA D-1833-2015
Lack of Assurance of Sterility
Class IIFDA: TerminatedMedistat RX LLC
10,690drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 289
10,690 detailed records are currently available in this category.
DrugOct 7, 2015
Apotex Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles recall — FDA D1834-2015
Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.
Class IIIFDA: TerminatedApotex Inc.
DrugOct 7, 2015
Guthy-Renker Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic recall — FDA D-0005-2016
Subpotent Drug: Salicylic acid is subpotent.
Class IIIFDA: TerminatedGuthy-Renker LLC
DrugOct 7, 2015
Guthy-Renker Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic recall — FDA D-0002-2016
Subpotent Drug: Salicylic acid is subpotent.
Class IIIFDA: TerminatedGuthy-Renker LLC
DrugOct 7, 2015
Guthy-Renker Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic recall — FDA D-0001-2016
Subpotent Drug: Salicylic acid is subpotent.
Class IIIFDA: TerminatedGuthy-Renker LLC
DrugOct 7, 2015
Hartley Medical Center Pharmacy Prolotherapy with Phenol recall — FDA D-1829-2015
Non-Sterility: Hartley Medical Center Pharmacy, Inc. is recalling Prolotherapy with Phenol due to non-sterility concerns.
Class IFDA: TerminatedHartley Medical Center Pharmacy, Inc.
DrugOct 7, 2015
Guthy-Renker Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic recall — FDA D-0004-2016
Subpotent Drug: Salicylic acid is subpotent.
Class IIIFDA: TerminatedGuthy-Renker LLC
DrugOct 7, 2015
Eagle Pharmacy LIPO B STERILE INJECTION 10 mL recall — FDA D-1832-2015
Subpotent Drug: trace amounts of methylcobalamin in compounded drug.
Class IIFDA: TerminatedEagle Pharmacy, Inc.
DrugSep 30, 2015
Pharmedium Services PHENYLephrine HCl, 60 mg added to 250 mL 0.9% Sodium Chloride Injection recall — FDA D-1827-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
LIDOCAINE HYDROCHLORIDE 1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose recall — FDA D-1815-2015
Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.
Class IIFDA: OngoingHospira, Inc.
DrugSep 30, 2015
Refresh Lacri-Lube recall — FDA D-1817-2015
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the…
Class IIFDA: TerminatedAllergan Sales, LLC
DrugSep 30, 2015
Allergan Sales FML recall — FDA D-1819-2015
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the…
Class IIFDA: TerminatedAllergan Sales, LLC
DrugSep 30, 2015
Allergan Sales BLEPHAMIDE recall — FDA D-1820-2015
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the…
Class IIFDA: TerminatedAllergan Sales, LLC
DrugSep 30, 2015
Pharmedium Services PHENYLephrine HCl, 50 mg added to 250 mL 0.9% Sodium Chloride Injection recall — FDA D-1821-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
Pharmedium Services PHENYLephrine HCl, 20 mg added to 250 mL 0.9% Sodium Chloride Injection recall — FDA D-1826-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
Pharmedium Services Fentanyl Citrate, 5 mcg per mL (1,250 mcg per 250 mL), 250 mL total recall — FDA D-1825-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
Pharmedium Services PHENYLephrine HCl, 10 mg added to 250 mL 0.9% Sodium Chloride Injection recall — FDA D-1828-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
Pharmedium Services PHENYLephrine HCl, 40 mg added to 250 mL 0.9% Sodium Chloride Injection recall — FDA D-1822-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
Refresh P.M recall — FDA D-1818-2015
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the…
Class IIFDA: TerminatedAllergan Sales, LLC
DrugSep 30, 2015
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG VIAFLEX Container recall — FDA D-1816-2015
Lack of Assurance of Sterility: Recalling firm reported a complaint for mold on the interior surface of the overpouch.
Class IIFDA: TerminatedBaxter Healthcare Corporation
DrugSep 30, 2015
Pharmedium Services Bupivacaine HCl 0.0625%, 250 mL total volume in a 250 mL LifeCare Bag in recall — FDA D-1823-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 30, 2015
Pharmedium Services Morphine Sulfate, 1 mg per mL (250 mg per 250 mL), 250 mL total volume recall — FDA D-1824-2015
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter…
Class IFDA: TerminatedPharmedium Services, LLC
DrugSep 23, 2015
The Compounding Pharmacy of Hydromorphone 80 mg/ml + Bupivacaine 10 mg/ml + Clonidine 1,000 recall — FDA D-1682-2015
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Class IIFDA: TerminatedThe Compounding Pharmacy of America
DrugSep 23, 2015
The Compounding Pharmacy of Morphine 50 mg/ml + Fentanyl 1,500 mcg/ml + Baclofen 800 mcg/ml recall — FDA D-1706-2015
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Class IIFDA: TerminatedThe Compounding Pharmacy of America
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.