Medical DeviceNov 20, 2024
The Metrix Company VYGON 100 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9601 recall — FDA Z-0330-2025
A limited number of IV bags have been found to leak during filling.
Class IIFDA: OngoingThe Metrix Company
November 2024 recalls — page 8
These records include useful source details for the selected month.
Medical DeviceNov 20, 2024
AVID Medical Halyard CYSTO PDS - Medical convenience kits recall — FDA Z-0402-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard UPPER EXTREMITY PACK - Medical convenience kits recall — FDA Z-0420-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Philips Respironics Trilogy Evo Universal Ventilator recall — FDA Z-0292-2025
Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow…
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard MANIFOLD CATH PACK - Medical convenience kits recall — FDA Z-0448-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Atlan A350XL recall — FDA Z-0305-2025
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Class IFDA: OngoingDraeger Medical, Inc.
Medical DeviceNov 20, 2024
The Metrix Company Imed Products Imed EVA BAG, 500 mL, 2-PORTS, REF IM68050 recall — FDA Z-0344-2025
A limited number of IV bags have been found to leak during filling.
Class IIFDA: OngoingThe Metrix Company
Medical DeviceNov 20, 2024
AVID Medical Halyard OPEN HEART PACK MAIN - Medical convenience kits recall — FDA Z-0387-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Topcon Medical Systems The IMAGEnet 6 Ophthalmic Data System is a software program that is recall — FDA Z-0362-2025
The overlay of visual field test locations on a probability map, as presented in IMAGEnet 6 in the so-called "Hood Report", is not appropriate as it can imply a structure/function…
Class IIFDA: OngoingTopcon Medical Systems, Inc.
Medical DeviceNov 20, 2024
MEDLINE INDUSTRIES, LP - Northfield Clean Catch Kit, SKU DYKM1833A recall — FDA Z-0354-2025
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceNov 20, 2024
MEDLINE INDUSTRIES, LP - Northfield URINE COLLECTION VHC, SKU DYLAB1016 recall — FDA Z-0359-2025
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceNov 20, 2024
AVID Medical Halyard OR ENDOVASCULAR TRAY - Medical convenience kits recall — FDA Z-0427-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile recall — FDA Z-0366-2025
There is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device…
Class IIFDA: OngoingStryker Corporation
Medical DeviceNov 20, 2024
AVID Medical Halyard CPT PEDS ADULT CH PACK - Medical convenience kits recall — FDA Z-0433-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
The Metrix Company SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports, REF 66040 recall — FDA Z-0335-2025
A limited number of IV bags have been found to leak during filling.
Class IIFDA: OngoingThe Metrix Company
Medical DeviceNov 20, 2024
AVID Medical Halyard KIT, TOTAL KNEE - Medical convenience kits recall — FDA Z-0394-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Bard Peripheral Vascular The EVSRF catheter is a sterile, single-use disposable medical recall — FDA Z-0371-2025
The Venclose" RF Ablation Catheters may have been manufactured with internal wiring error. The red and yellow signal wires were soldered on swapped ports of the catheter PCB. This error in…
Class IIFDA: OngoingBard Peripheral Vascular Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard PACEMAKER PK - Medical convenience kits recall — FDA Z-0454-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard KIT, TOTAL KNEE - Medical convenience kits recall — FDA Z-0390-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard D & C PACK-CKC - Medical convenience kits recall — FDA Z-0385-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
The Metrix Company SECURE 250 mL EMPTY EVA CONTAINER With 2 Ports, REF 66045 recall — FDA Z-0339-2025
A limited number of IV bags have been found to leak during filling.
Class IIFDA: OngoingThe Metrix Company
Medical DeviceNov 20, 2024
Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Non-coated, 70mm - Designed recall — FDA Z-0367-2025
There is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device…
Class IIFDA: OngoingStryker Corporation
Medical DeviceNov 20, 2024
AVID Medical Halyard KIT, CARDIAC ROBOTIC - Medical convenience kits recall — FDA Z-0392-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
MEDLINE INDUSTRIES, LP - Northfield Lab Kit, SKU DYLAB1018 recall — FDA Z-0355-2025
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged…
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.