Home › BURLINGTON MEDICAL, LLC › F125
F125
BURLINGTON MEDICAL, LLC · Model STLF111-MF · UDI-DI 00840331203530
6
510(k) clearances
115
Adverse events (1 deaths)
25
Recalls
29
Facilities
Description
STLF111-MF (F111: 1 Piece Wrap Around with Wide Stretch Belt .35MM TRUELITE, MF)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
| 2019-06-07 | Burlington Medical, LLC | The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to s |
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.