Home › Caldera Medical, Inc. › Vertessa Lite Y-mesh 22x4x3cm
Vertessa Lite Y-mesh 22x4x3cm
Caldera Medical, Inc. · Model CAL-VL2243 · UDI-DI 00890594000421
OTO
Prescription
1
510(k) clearances
4,780
Adverse events (24 deaths)
1
Recalls
20
Facilities
Description
Vertessa Lite Y 22x4x3cm polypropylene mesh for sacrocolpopexy
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-04-12 | Coloplast Manufacturing US, LLC | Coloplast is recalling one lot of Restorelle L prosthesis because it is mislabeled. The incorrect Instructions For Use (IFU) pamphlet is included in the packaging. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.