Ultra Clean Systems, Inc. recalls Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning system
During routine preventative maintenance checks, it was revealed that carbon filter sensors were breaking down due to electrochemical degradation.
Read the official notice →- Date
- 2025-06-04
- Country
- United States
- Brand
- Ultra Clean Systems, Inc.
- Product
- Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning system
- Classification
- Class II
- Units
- Worldwide - U.S. Nationwide distribution including in the states of AZ, 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2025-06-04
USStraumann USA LLC recalls GM Helix Acqua Implant, Article Number: 140.984
It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead.
FDA · DeviceStraumann USA LLCWorldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, Il…Official notice →- US
Straumann USA LLC recalls Plus Initial Drill, Article Number: 103.170;
The referred batch was produced without the laser engraving of 7 mm.
FDA · DeviceStraumann USA LLCWorldwide - US Nationwide distribution in the states of AZ, CA, FL, GA, IL,…Official notice → - US
Pro-Med Instruments Gmbh recalls DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
Potential of compromised compatibility resulting in influence on the positioning of the reference array and an influence of the function of the navigation system cannot be excluded.
FDA · DevicePro-Med Instruments GmbhWorldwide - US Nationwide distribution in the states of CA, CO, KY, ID, IL,…Official notice → - US
C-RAD POSITIONING AB recalls Brand Name: Catalyst+ Product Name: C4D software used in conjunction with Catalyst (SP001-0025), Catalyst HD (SP001-0026), Catalyst PT…
Software issue with scanning equipment that can results in the filed rotation not being applied correctly.
FDA · DeviceC-RAD POSITIONING ABWorldwide - US Nationwide distribution in the states of AK, FL, WA, VA, WA,…Official notice → - US
Onkos Surgical, Inc. recalls ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of ELEOS Limb Salvage System
Potential challenge with intraoperative assembly of the external taper of a single midsection with the internal taper of a mating proximal femur.
FDA · DeviceOnkos Surgical, Inc.US Nationwide distribution in the states of AZ, CA, FL, FL, MD, MO, NC, TN.Official notice → - US
Prismatik Dentalcraft, Inc. recalls Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The…
Due to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.
FDA · DevicePrismatik Dentalcraft, Inc.U.S Nationwide distribution in the states of KY, MA, MI, NC, VA, and WV.Official notice →