Home › MEDTRONIC XOMED, INC. › Merocel®
Merocel®
MEDTRONIC XOMED, INC. · Model 400250 · UDI-DI 20681490104795
LYA
Prescription
10
510(k) clearances
203
Adverse events (3 deaths)
2
Recalls
105
Facilities
Description
RETRACTOR COVER 400250 10PK 2.5CM DEAVER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-07-27 | GELITA MEDICAL GMBH | In routine bioburden testing, higher than acceptable levels of Endotoxins were observed. |
| 2006-07-11 | Porex Surgical, Inc. | Device contains a trace amount of amine via introduction through an intermediate supplied by a third party raw material |
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.