Preat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with…
Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.
Read the official notice →- Date
- 2025-06-25
- Country
- United States
- Brand
- Preat
- Product
- Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with…
- Classification
- Class II
- Units
- U.S. Nationwide distribution in the states of AZ, CA, GA, MO, NJ, NY, OH, PA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Preat recalls
- 2025-09-10
USPreat Corp recalls NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662
Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the…
FDA · DevicePreat CorpUS Nationwide distribution in the states of NY, FL, PA, CA, OH.Official notice →- 2025-07-16
- US
Preat Corp recalls Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
FDA · DevicePreat CorpUS Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY,…Official notice → - 2024-08-28
- US
Preat Corp recalls Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann…
Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.
FDA · DevicePreat CorpU.S. Nationwide distribution in the states of AK, AZ, FL, GA, IL, LA, MD, MI,…Official notice → - 2024-07-17
- US
Preat Corp recalls 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture…
Due to incorrect milled titanium abutment being packaged and labeled.
- 2024-03-27
- US
Preat Corp recalls Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
- 2023-11-01
- US
Preat Corp recalls Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
Other drugs & medical recalls in the United States
- 2025-06-25
- US
Fresenius Medical Care Holdings, Inc. recalls 5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline,…
Potential of blood leak occurring between the lower port of the venous chamber and the tubing include: hemodiafiltration (HDF), hemodialysis (HD), hemofiltration (HF), and isolated ultrafiltration.
FDA · DeviceFresenius Medical Care Holdings, Inc.US Nationwide distribution in the state of Massachusetts.Official notice → - US
ICU Medical, Inc. recalls ICU Medical Plum Solos, Item number 400011001; infusion pump
Internal testing found that Plum Duo pumps with software version 1.1.1 have a workflow that may result in bypassing the Maximum Dose Limit alert. The Maximum Dose Limit is set in the LifeShield Drug Library Manager…
FDA · DeviceICU Medical, Inc.Worldwide - US Nationwide distribution in the states of FL, KY, VA, MS, MA,…Official notice → - US
BALT USA, LLC recalls Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694…
Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification.
FDA · DeviceBALT USA, LLCWorldwide - U.S. Nationwide distribution including in the states of AL, AR,…Official notice → - US
Chamberlain Technologies LLC recalls SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
Potential presence of residual adhesive material on the mesh surface.
FDA · DeviceChamberlain Technologies LLCUS distribution to states of: Illinois, Nebraska, & CaliforniaOfficial notice → - US
Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia Max. Model Number: 10762473
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
- US
Ohio Medical Corporation recalls GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
Erroneous calibration values, potentially resulting in: as the device ages, oxygen purity will gradually decrease to the point where the device alarms to indicate low oxygen purity will be incorrect.
FDA · DeviceOhio Medical CorporationUS Nationwide distribution in the states of AR, FL, VA, ND, MS, MN, CA, NV, KY.Official notice →