Pro-Med Instruments Gmbh 2025-06-04 Health serious FDA
Health · FDA · Recall #FDA-Z-1860-2025
DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002) Recall
Issued June 4, 2025 · Pro-Med Instruments Gmbh
In June 2025, Pro-Med Instruments Gmbh recalled the DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002), a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002) right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Pro-Med Instruments Gmbh 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
- Pro-Med Instruments Gmbh
- Category
- Health
- Recall date
- June 4, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution in the states of CA, CO, KY, ID, IL, MA, MO, NC, NJ, NY, TX and the countries of Algeria, Argentina,
- Recall number
- FDA-Z-1860-2025
- Made in
- Germany
- Issuing agency
- FDA
In context
- Pro-Med Instruments Gmbh has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.