Home › BURLINGTON MEDICAL, LLC › F111
F111
BURLINGTON MEDICAL, LLC · Model UBF111XSF · UDI-DI 00840186673595
6
510(k) clearances
114
Adverse events (1 deaths)
25
Recalls
29
Facilities
Description
WRAPCB-UBF111-XSF (CUSTOM: F111, .25MM BURLITE, XSF)
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.