X-NAV Technologies, LLC recalls X-Guide Handpiece Adaptor Sleeve 3, Model P010727
The Handpiece Adaptor may have a manufacturing defect causing incorrect geometry. The incorrect geometry in turn causes the Handpiece Adaptor to not fit onto the doctor's dental handpiece.
Read the official notice →- Date
- 2024-04-10
- Country
- United States
- Brand
- X-NAV Technologies
- Product
- X-Guide Handpiece Adaptor Sleeve 3, Model P010727
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of China, Europe,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 X-NAV Technologies recalls
- 2022-11-16
USX-NAV Technologies, LLC recalls X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog…
Product missing one of two welds connecting the tip to the shaft, if the remaining weld breaks, it is possible that the tip could fall out during X-Mark registration and fall into the patient s mouth. In this case, the…
FDA · DeviceX-NAV Technologies, LLCUS Nationwide distribution and Foreign country of: CanadaOfficial notice →
Other drugs & medical recalls in the United States
- 2024-04-10
- US
Baxter Healthcare Corporation recalls Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention and/or…
Inconsistencies were identified with service records associated with corrections performed for a previous Medical Device Correction issued by Baxter (ref number: FA-2022-026). Your devices have been identified as…
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the state of Colorado.Official notice → - US
Becton Dickinson & Co. recalls BD Phoenix Yeast ID Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray)…
Esculin, a substrate used in other panels and normally in A16 well, was found in A17 well. A17 in yeast panels is supposed to be an empty well and is not a part of the normal ID evaluation. However, A17 is checked for…
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of AR, BE, CO, IN,…Official notice → - US
Becton Dickinson & Co. recalls BD Phoenix NMIC-306 Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray)…
Products were found to have confirmed drug cross contamination prior to release may lead to incorrect, inadequate, or absent antibiotic treatment or delay in results
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of AR, BE, CO, IN,…Official notice → - US
SleepNet Corporation recalls Mojo 2 Full Face AAV Non Vented Mask, All Sizes
Update to contraindications and warning language due to CPAP masks containing magnets.
FDA · DeviceSleepNet CorporationWorldwide distribution - US Nationwide and the countries of AUSTRIA, BAHRAIN,…Official notice → - US
SSM Health Care St. Louis DBA SSM St. Clare Health Center recalls Phenylephrine HCl, 1000 mcg/10 mL, 10 mL Total Volume per syringe, Intravenous, Rx Only,…
Lack of Assurance of Sterility: Firm did not perform process validation.
- US
X-Gen Pharmaceuticals Inc. recalls Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After…
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg…