DrugNov 9, 2022
Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30-count bottles recall — FDA D-0024-2023
Presence of Foreign Substance
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
November 2022 recalls — page 10
These records include useful source details for the selected month.
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder VORICONAZOLE OPTH SOLUTION 2% STERILE SOLN, 10 recall — FDA D-0057-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PAPAVERINE/PHENTOLAMINE/PROSTAGLANDIN INJ recall — FDA D-0048-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN INJ recall — FDA D-0044-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder SERUM TEARS IN NSAL 20% OPTH SOLUTION, 3 mL recall — FDA D-0054-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder METHYLCOBALAMIN PF 1 ML Injection Solution recall — FDA D-0038-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder CEFUROXIME INTRAVITREAL SYR 1MG/0.1ML Solution recall — FDA D-0031-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PRED ACETATE / GATIFLOXACIN 1% / 0.5% SUSP, 10 recall — FDA D-0051-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PAPAVERINE/PHENTOLAMINE/PROSTAGLANDIN INJ recall — FDA D-0049-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder LAURETH-9 INJ 2% Solution, 30 ML vial recall — FDA D-0034-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PHENTOLAMINE 10MG/ML INJECTION, 10MG/ML recall — FDA D-0050-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PAPAVERINE / PHENTOLAMINE INJECTION 150MG / recall — FDA D-0046-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder TALC, STERILE POWDER, 5 GM vial recall — FDA D-0055-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN INJ recall — FDA D-0043-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder ACETYLCYSTEINE OPTH 10% Solution, 15 mL recall — FDA D-0026-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Susvimo (ranibizumab injection), 100mg/mL, sold together as a) carton containing One Susvimo recall — FDA D-0025-2023
Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it…
Class IIIFDA: TerminatedGenentech Inc.
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder GLYCERIN OPHTHALMIC DROPS 98.5% Solution, 10 recall — FDA D-0033-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder PAPAVERINE HCL STOCK SOLUTION 30MG/ML recall — FDA D-0047-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder MOXIFLOXACIN PRESERVATIVE FREE SYR, 0.15 recall — FDA D-0040-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
DrugNov 9, 2022
Pharmacy Plus, Inc. dba Vital Care Compounder MEDROXYPROGESTERONE ACETATE 300 MG/ML recall — FDA D-0037-2023
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Class IIFDA: OngoingPharmacy Plus, Inc. dba Vital Care Compounder
VehicleNov 3, 2022
Bronco camera recall — NHTSA campaign 22V825000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles equipped with rearview camera systems and 8-inch screen displays. The rearview camera image may still be displayed…
cameraFord Motor Company
VehicleNov 3, 2022
General Motors lighting control module software recall — NHTSA campaign 22V827000
General Motors, LLC (GM) is recalling certain 2021 Yukon, Yukon XL, Chevrolet Tahoe, Chevrolet Suburban, Cadillac Escalade, and Cadillac Escalade ESV vehicles. The daytime running lights…
lighting control module softwareGeneral Motors, LLC
Medical DeviceNov 2, 2022
MEDLINE 24 BLOOD CLUTURE KIT, Reorder #: DYNDH1632 recall — FDA Z-0123-2023
Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceNov 2, 2022
MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592 recall — FDA Z-0122-2023
Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.