Class IIOngoingZ-2862-2026
Stryker Corporation recalls STRYKER AHTO TUBE SET PACKAGING
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Stryker CorporationCAAug 12, 2026
All device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 241–252 of 4,996 recalls
Class IIOngoingZ-2861-2026
Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/C…
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).
Nuclein LLCTXAug 12, 2026
Class IIOngoingZ-2860-2026
Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400…
Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperativ…
Maquet Critical Care A…Aug 12, 2026
Class IIOngoingZ-2859-2026
Innovasis, Inc recalls Anti-Torque
Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with undersized condition which could prevent mat…
Innovasis, IncUTAug 12, 2026
Class IIOngoingZ-2858-2026
Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequen…
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
Medical Action Industr…NCAug 12, 2026
Class IIOngoingZ-2857-2026
Oxos Medical Inc recalls Brand Name: OXOS Medical
Due to a defective circuit board that overheats
Oxos Medical IncGAAug 12, 2026
Class IIOngoingZ-2856-2026
MUNEVO GMBH recalls munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Applicatio…
A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control while driving the wheelchair.…
MUNEVO GMBHAug 12, 2026
Class IIOngoingZ-2855-2026
THERANICA BIOELECTRONICS LTD recalls Nerivio Infinity. Model/Catalog Number: FGD000100. Software Version: FW Version 4.1.2.0
Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor.
- Distal Transcutaneous Electrical Stimulator For Treatment Of Acute Migraine
- Component design/selection
THERANICA BIOELECTRONI…Aug 12, 2026
Class IIOngoingZ-2854-2026
Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Versio…
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Copan WASPAug 12, 2026
Class IIOngoingZ-2853-2026
Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum R…
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use.…
Pride Mobility Product…PAAug 12, 2026
Class IIOngoingZ-2852-2026
Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software…
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use.…
Pride Mobility Product…PAAug 12, 2026
Class IIOngoingZ-2851-2026
Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: Quantum 4Front 2HD Model/Catalog Number: Quan…
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use.…
Pride Mobility Product…PAAug 12, 2026