S S C O R Inc SSCOR Suction Device Model 2310BV Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SSCOR Suction Device Model 2310BV
Brand
S S C O R Inc
Lot Codes / Batch Numbers
Serial Numbers: C00575 - C00624 (found on a silver label on the back of each device)
Products Sold
Serial Numbers: C00575 - C00624 (found on a silver label on the back of each device)
S S C O R Inc is recalling SSCOR Suction Device Model 2310BV due to Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in quest. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
Recommended Action
Per FDA guidance
SSCOR Powered Suction Device not performing as intended.
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 noticeDistribution
As reported by FDA
CA, FL, IL, IN, IA, KY, MO, NJ, NY, NC, OH
Page updated: Jan 10, 2026