DrugFeb 22, 2023
Leadiant Biosciences Abelcet recall — FDA D-0327-2023
Lack of assurance of sterility: Medial fill with presence of Cupriavidus pauculus.
Class IIFDA: TerminatedLeadiant Biosciences, Inc.
February 2023 recalls — page 3
These records include useful source details for the selected month.
DrugFeb 22, 2023
Sentara Infusion Services CEFAZOLIN (a) 12GM IN NS 600ML, (b) 2GM IN NS 100ML, (c) 2GM/20ML recall — FDA D-0278-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
DrugFeb 22, 2023
Sentara Infusion Services MEROPENEM (a) 1000MG IN NS 250ML, (b) 2GM IN NS 100ML, (c) 500mg recall — FDA D-0303-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
DrugFeb 22, 2023
HTO Nevada Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive recall — FDA D-0271-2023
cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.
Class IIFDA: TerminatedHTO Nevada, Inc.
DrugFeb 22, 2023
Sentara Infusion Services CEFEPIME, (a) 2GM IN NS 100ML (b)8GM IN NS 400ML (c) 12GM IN NS recall — FDA D-0280-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
DrugFeb 22, 2023
Sentara Infusion Services TPN 107gm/AA, 200gm/DEX, 50gm/LIP 2250mL, (b) 108GM/AA, 330GM/DEX recall — FDA D-0319-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
DrugFeb 22, 2023
McGuff Compounding Pharmacy Services Thiamine Hydrochloride 200 mg/2mL (100mg/mL) recall — FDA D-0266-2023
Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Class IIFDA: TerminatedMcGuff Compounding Pharmacy Services, Inc.
DrugFeb 22, 2023
Sentara Infusion Services TPN (a) 100GM/AA, 285GM/DEX, (b)55GM/LIP 2300ML, (c)55GM/AA recall — FDA D-0318-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
DrugFeb 22, 2023
Sentara Infusion Services TPN (a) 95GM/AA, 385/DEX, 50GM/LIP 1800ML, (b)TPN AA:100GM recall — FDA D-0321-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
DrugFeb 22, 2023
Sentara Infusion Services HYDROMORPHONE (a) 1MG/ML IN NS, 50ML, 75 ML, 100ML, 175ML recall — FDA D-0296-2023
Lack of sterility assurance
Class IIFDA: TerminatedSentara Infusion Services
VehicleFeb 16, 2023
CR-V recliner recall — NHTSA campaign 23V092000
Honda (American Honda Motor Co.) is recalling certain 2023 CR-V vehicles. The front passenger seat back frame may not have been welded properly, which can cause the seat back position to…
reclinerHonda (American Honda Motor Co.)
VehicleFeb 16, 2023
Nissan key/sender recall — NHTSA campaign 23V093000
Nissan North America, Inc. (Nissan) is recalling certain 2014-2020 Rogue and 2017-2022 Rogue Sport vehicles equipped with a jackknife style ignition key. The jackknife key may collapse into…
key/senderNissan North America, Inc.
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1073-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
Roche Molecular Systems cobas SARS-CoV-2 & Influenza A/B Qualitative assay for use on the recall — FDA Z-1104-2023
The firm received customer complaints regarding false negative Influenza A (Flu A) results and late Flu A Target Ct values. A false negative influenza A result may lead to additional…
Class IIFDA: OngoingRoche Molecular Systems, Inc.
Medical DeviceFeb 15, 2023
Roche Molecular Systems cobas Influenza A/B & RSV UC (Utility Channel) Qualitative nucleic recall — FDA Z-1106-2023
The firm received customer complaints regarding false negative Influenza A (Flu A) results and late Flu A Target Ct values. A false negative influenza A result may lead to additional…
Class IIFDA: OngoingRoche Molecular Systems, Inc.
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1088-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING GE Nuclear Medicine 600/800 series systems recall — FDA Z-1053-2023
A mitigation may not be correctly implemented. If this is the case, the detector can fall, leading to life-threatening bodily injury.
Class IFDA: OngoingGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1069-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1068-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
Olympus Corporation of the Americas SPiN Thoracic Navigation System Model: SYS-4000 recall — FDA Z-1103-2023
A grainy image is observed when using a SPiN Vision Single-Use Flexible Bronchoscope (models INS-7100 or INS-7130) with the SYS-4000 system due to an incorrect DVI cable supplied may result…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1076-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1096-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1090-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: IM recall — FDA Z-1082-2023
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
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.