W&H DENTALWERK BUERMOOS GMBH recalls W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000
1:2 speed increasing surgical handpieces have been incorrectly laser marked during production. The specific laser marking should read 1:2, but instead it reads 1:1 on the body of the handpiece
Read the official notice →- Date
- 2024-02-28
- Country
- United States
- Brand
- W&H DENTALWERK BUERMOOS GMBH
- Product
- W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Canada, Australia,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2024-02-28
USIMPULSE DYNAMICS (USA) INC recalls OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Smart Mini and Lite
OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly detects a charging error. This may cause patients to experience heart failure symptoms similar to before implantation of the device.
FDA · DeviceIMPULSE DYNAMICS (USA) INCDomestic US distribution nationwide. International distribution to Austria…Official notice →- US
FUJIFILM Healthcare Americas Corporation recalls Synapse Cardiology PACS V7.3.0, V7.2, V7.1, V7.0. A web-based application as the primary user interface for the…
The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in a variance in the mass of the left ventricle (LV Mass). If used as a main factor for diagnosis, there is a risk of misdiagnosis or incorrect…
FDA · DeviceFUJIFILM Healthcare Americas CorporationUS domestic distribution nationwide. International distribution to Israel.Official notice → - US
3M Company - Health Care Business recalls 3M Specialty Blade Assembly, REF 9660,70-2011-8462-2, 7100213114, used with used with 3M Surgical Clipper Catalog Number 9661L
3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in minor injury: " Do not use on injured skin. " Do not leave…
- US
Olympus Corporation of the Americas recalls ESG PK CUTTING FORCEPS, 5MM, 33CM
The jaw may fracture prior to the procedure during the inspection instructed per the IFU, or during the procedure.
FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of Australia, Canada,…Official notice → - US
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules) used…
Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide Distribution: US nationwide including states of: AL, AK, AR, AZ, CA,…Official notice → - US
Canon Medical System, USA, INC. recalls The INFX-8000F is designed to take advantage of the latest technological innovations to reduce dose and to save time. A…
VAREX changed the manufacturing of the internal board, and the detectors displayed abnormal images. Internal board of the X-ray flat panel detector may display abnormal images, such as horizontal stripes, which may…