AMO Manufacturing USA, LLC 2022-01-05 Health serious FDA
Health · FDA · Recall #FDA-Z-0443-2022
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan… Recall
Issued January 5, 2022 · AMO Manufacturing USA, LLC
In January 2022, AMO Manufacturing USA, LLC recalled the iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Aberrometer and precision laser systems are affected by a remote code execution vulnerability existing when the Microsoft Windows Print Spooler service is enabled, and improperly performs privileged file operations. This could be exploited to run arbitrary code with SYSTEM privileges, allowing for program installation; view/change/deleting data; or creation of new accounts with full user rights.
What you should do
- 1 Stop using iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact AMO Manufacturing USA, LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- AMO Manufacturing USA, LLC
- Category
- Health
- Recall date
- January 5, 2022
- Units affected
- Not reported
- Sold at
- US: CA, TX, FL, LA, MD, IA, MA, VA, SD, MN, MO, NC, TN, SC, WA, NV, OH, KY, IN, CO, NJ, OK, NH, UT, AR, NY, AK, ND, NE, IL, AL, HI, CT, DE,
- Recall number
- FDA-Z-0443-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- AMO Manufacturing USA, LLC has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.