SA3, LLC recalls Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm
Due to failure of microbial testing for total aerobic microbial count (TAMC).
Read the official notice →- Date
- 2022-04-13
- Country
- United States
- Brand
- SA3, LLC
- Product
- Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm
- Classification
- Class II
- Units
- U.S. Nationwide distribution in the states of CA, FL and GA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-04-13
US
Stradis Medical, LLC dba Stradis Healthcare recalls Coryell Memorial Hosp Total, Joint Pack - Surgical Kit
The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.
FDA · DeviceStradis Medical, LLC dba Stradis HealthcareUS Nationwide distribution in the states of IN, TX, and PA.Official notice →US
Remote Diagnostic Technologies Ltd. recalls Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693
Distribution of Defibrillators that are not approved or cleared for distribution US Market.
FDA · DeviceRemote Diagnostic Technologies Ltd.US Nationwide distribution in the states of IL and KS.Official notice →US
GE Healthcare, LLC recalls Signa 1.5T TwinSpeed Magnetic Resonance Imaging System
There is potential for the images to be flipped left to right.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution. US nationwide, Argentina, Australia, Azerbaijan,…Official notice →US
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
US
Philips Healthcare recalls Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x
Due to an incorrect configuration setting in the EPX database of StentBoost Live, acquisition does not stop automatically as it should. When the user selects the StentBoost Live protocol on the Philips Azurion system,…
US
Siemens Medical Solutions USA, Inc recalls YSIO X.Pree
For the automated multi-image-acquisition procedure Ortho x-ray collimation is set in a preparative stage for the entire examination area prior to the exam. During acquisition of each individual x-ray image, the x-ray…
FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide, Worldwide distributionOfficial notice →