Home › Rochester Medical Corporation › FemSoft® Insert Female Urethral Insert
FemSoft® Insert Female Urethral Insert
Rochester Medical Corporation · Model 70200 · UDI-DI 00801741011122
OCK
Prescription
0
510(k) clearances
7
Adverse events
8
Recalls
0
Facilities
Description
Female Urethral Insert
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
| 2010-04-27 | Rochester Medical Corp | Rochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a small number of packages |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.