Z-0411-05

SSCOR Suction Device Model 2310BV

Name: Z-0411-05 SSCOR Suction Device Model 2310BV
Creator: S S C O R Inc
Published: 2005-01-06
License: https://open.fda.gov/license/

Sscor, Inc. / initiated 2005-01-06 / Terminated

FDA source

S S C O R Inc began a recall of SSCOR Suction Device Model 2310BV on 2005-01-06. The reason FDA records is "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". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0411-05
Status: Terminated
Initiated: 2005-01-06
Posted: 2005-01-27
Terminated: 2011-06-13
Recalling firm: Sscor, Inc.
Product: SSCOR Suction Device Model 2310BV
Product code: BTA Pump, Portable, Aspiration (Manual Or Powered)
Reason for recall: 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.
FDA root cause: Other
Action: SSCOR Powered Suction Device not performing as intended.
Quantity in commerce: 39
Distribution: CA, FL, IA, IL, IN, KY, MO, NC, NJ, NY, OH, France, New Zealand, Singapore, United Kingdom
Product codes and lots: Serial Numbers: C00575 - C00624 (found on a silver label on the back of each device)

Product code BTA

K945929Class IIS-Scort(r)duet Model 2014 Portable Suction PumpSscor / cleared 1994-12-22

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)