Home › Smith & Nephew, Inc. › PROFIX
PROFIX
Smith & Nephew, Inc. · Model 71508147 · UDI-DI 03596010220899
KWH
Prescription
10
510(k) clearances
149
Adverse events
2
Recalls
33
Facilities
Description
PROFIX CONFORMING PLUS TIBIAL INSERT RIGHT SIZE 4 25MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-04-06 | Tornier, Inc. | Tornier, Inc. has received a report of a mislabeled product due to a product mix-up. The package label indicated that the product was a model LMP-50 however the product inside the |
| 2009-03-01 | Sgarlato Med, LLC | Products with an expiration date of August, 2009 were labeled with an expiration date of May 2013. Additionally, the outer packages were labeled with an incorrect lot number. The o |
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.
