Home › BIO-RAD LABORATORIES, INC. › Quantase
Quantase
BIO-RAD LABORATORIES, INC. · Model 532-5040 · UDI-DI 00847817021527
1
510(k) clearances
0
Adverse events
2
Recalls
2
Facilities
Description
Quantase Neonatal Accessory Kit 5 Elution Buffer
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-11-26 | Perkinelmer | Truncated V-Bottomed Microplate Wells used in assays contain defective wells. |
| 2010-01-26 | Bio-Rad Laboratories Inc | Pressure contained within the Elution Buffer vial may expel the rubber stopper, causing the potential for injury. |
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.
