Home › MEDLINE INDUSTRIES, INC. › MEDLINE
MEDLINE
MEDLINE INDUSTRIES, INC. · Model 2318R · UDI-DI 10193489020458
NLF
Prescription
1
510(k) clearances
89
Adverse events
3
Recalls
19
Facilities
Description
2318 @LNCS PEDIATRIC PULSE OX SENSOR 3FT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-03-11 | Ascent Healthcare Solutions, Inc. | Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products. |
| 2008-03-11 | Ascent Healthcare Solutions, Inc. | Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products. |
| 2008-03-11 | Ascent Healthcare Solutions, Inc. | Sterility Compromised -- Ascent Healthcare Solutions cannot validate the sterilization process for a variety of Ascent Healthcare Solutions products. |
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.