Innovasis, Inc recalls Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
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…
Read the official notice →- Date
- 2026-08-12
- Country
- United States
- Brand
- Innovasis
- Product
- Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
- Classification
- Class II
- Units
- US Nationwide distribution in the states of TX, CA.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Innovasis recalls
- 2024-09-25
USInnovasis, Inc recalls TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion device intended to…
Due to interfacing issues between the implant trial and inserter of the lumbar intervertebral fusion device.
FDA · DeviceInnovasis, IncU.S. Nationwide distribution in the states of AL, CA, CO, FL, ID, MI, SD, TX…Official notice →
Other drugs & medical recalls in the United States
- 2026-08-12
- US
Stryker Corporation recalls STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
FDA · DeviceStryker CorporationWorldwide distribution - US Nationwide and the countries of Australia, Brazil,…Official notice → - US
Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2…
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).
- US
Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540…
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…
FDA · DeviceMaquet Critical Care ABWorldwide - US Nationwide distribution to the states of AL, AR, CA, CO, DC,…Official notice → - US
Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of CA.Official notice → - US
Oxos Medical Inc recalls Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product…
Due to a defective circuit board that overheats
FDA · DeviceOxos Medical IncUS Nationwide distribution in the states of FL, GA, IN, SC, TX, VA.Official notice → - US
MUNEVO GMBH recalls munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
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. The…
FDA · DeviceMUNEVO GMBHWorldwide - US Nationwide distribution in the states of California, Florida,…Official notice →