Rultract Inc Rultract Surgical Retractor, 4100 Series, all system configurations, reusable. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Rultract Surgical Retractor, 4100 Series, all system configurations, reusable.
Brand
Rultract Inc
Lot Codes / Batch Numbers
S/Ns: 0001 to 2005, and S/Ns: 2172 to 2885
Products Sold
S/Ns: 0001 to 2005, and S/Ns: 2172 to 2885
Rultract Inc is recalling Rultract Surgical Retractor, 4100 Series, all system configurations, reusable. due to Component spring or nut may loosen, detach, and fall into chest of patient during surgical procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Component spring or nut may loosen, detach, and fall into chest of patient during surgical procedure.
Recommended Action
Per FDA guidance
The firm notified their affected consignees by letter on 9/18/2003.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026