FDA Device Intelligence
HomeMp Biomedicals, LLC › MP Biomedicals LLC

MP Biomedicals LLC

Mp Biomedicals, LLC · Model 07553306 · UDI-DI 00817830023129

JIA
1
510(k) clearances
0
Adverse events
6
Recalls
2
Facilities

Description

NEONATAL GALACTOSE MW 10 PLATE ENZYME ASSAY KIT (WITH MEMBRANE)

Recalls

DateFirmReason
2004-09-08PerkinElmer LAS IncThere is an increase in the number of normal specimen results below the lowest calibrator and based on a report that the normal controls were running low, sometimes out of the spec
2004-01-09Perkin Elmer Life and Analytical Sciences IncThe device is not stable throughout its labeled expiration date.
2004-01-09Perkin Elmer Life and Analytical Sciences IncThe device is not stable throughout its labeled expiration date.
2003-05-30PerkinElmer Life Sciences IncThe device is not stable throughout its labeled expiration date.
2003-05-30PerkinElmer Life Sciences IncThe device is not stable throughout its labeled expiration date.
2003-05-30PerkinElmer Life Sciences IncThe device is not stable throughout its labeled expiration date.

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 docs
Data 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.