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
Monthly breakdown
2023 recalls by month
Select a month to review the recall records reported during that period.
December 2023295 records · 4 categoriesNovember 2023387 records · 4 categoriesOctober 2023214 records · 4 categoriesSeptember 2023253 records · 4 categoriesAugust 2023478 records · 4 categoriesJuly 2023263 records · 4 categoriesJune 2023339 records · 4 categoriesMay 2023410 records · 4 categoriesApril 2023189 records · 4 categoriesMarch 2023788 records · 4 categoriesFebruary 2023253 records · 4 categoriesJanuary 2023205 records · 4 categories
2023 recalls — page 154
Records are ordered by the best available source date.
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
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1097-2023
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-1056-2023
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
TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile recall — FDA Z-1107-2023
The device is breaking and falling off the Nuvasive T-Handle with Hudson Adapter on certain Nuvasive XLIF instruments during surgery when malleted.
Class IIFDA: OngoingTrackx Technology Inc.
Medical DeviceFeb 15, 2023
MEDLINE INDUSTRIES, LP - Northfield Sterile Procedural Trays, labeled as the following: a recall — FDA Z-1078-2023
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 ANCILLARY PACK-LF. Sterile Procedural Tray recall — FDA Z-1060-2023
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-1091-2023
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 TRACH PACK. Sterile Procedural Tray recall — FDA Z-1061-2023
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: DR recall — FDA Z-1086-2023
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
About the 2023 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.